Self-Contained Breathing Apparatus Remaining Service-Life Indicator Performance Requirements, 2618-2622 [2013-00371]
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Federal Register / Vol. 78, No. 9 / Monday, January 14, 2013 / Rules and Regulations
therefore it is categorically excluded
from further review under paragraph
34(g) of Figure 2–1 of the Commandant
Instruction. An environmental analysis
checklist supporting this determination
and a Categorical Exclusion
Determination are available in the
docket where indicated under
ADDRESSES. We seek any comments or
information that may lead to the
discovery of a significant environmental
impact from this rule.
List of Subjects in 33 CFR Part 165
Harbors, Marine safety, Navigation
(water), Reporting and recordkeeping
requirements, Security measures,
Waterways.
For the reasons discussed in the
preamble, the Coast Guard amends 33
CFR part 165 as follows:
PART 165—REGULATED NAVIGATION
AREAS AND LIMITED ACCESS AREAS
commissioned, warrant or petty officer
who has been designated by the Captain
of the Port, Sector Lake Michigan to act
on his behalf.
(4) Vessel operators desiring to enter
or operate within the safety zone shall
contact the Captain of the Port, Sector
Lake Michigan or his on-scene
representative to obtain permission to
do so. The Captain of the Port, Sector
Lake Michigan or his on-scene
representative may be contacted via
VHF Channel 16. Vessel operators given
permission to enter or operate in the
safety zone must comply with all
directions given to them by the Captain
of the Port, Sector Lake Michigan, or his
on-scene representative.
Dated: December 28, 2012.
J.W. Davenport,
Commander, U.S. Coast Guard, Acting
Captain of the Port, Sector Lake Michigan.
[FR Doc. 2013–00514 Filed 1–11–13; 8:45 am]
BILLING CODE 9110–04–P
1. The authority citation for part 165
continues to read as follows:
■
Authority: 33 U.S.C. 1231; 46 U.S.C.
Chapters 701, 3306, 3703; 50 U.S.C. 191, 195;
33 CFR 1.05–1, 6.04–1, 6.04–6, and 160.5;
Pub. L. 107–295, 116 Stat. 2064; Department
of Homeland Security Delegation No. 0170.1.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
2. Add § 165.T09–1099 to read as
follows:
RIN 0920–AA38
■
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§ 165.T09–1099 Safety Zone; Bridge
Demolition Project, Indiana Harbor Canal,
East Chicago, Indiana.
(a) Location. The safety zone will
encompass all waters of the Indiana
Harbor Canal in the vicinity of the Cline
Avenue Bridge at approximate position
41°39′4.3″ N and 87°27′54.3″ W (NAD
83).
(b) Effective and Enforcement Period.
This rule is effective from 12:00 p.m. on
January 1, 2013 until 12:00 a.m. on
February 1, 2013. The Captain of the
Port, Sector Lake Michigan, will
establish enforcement dates that will be
announced with a Notice of
Enforcement and marine information
broadcasts.
(c) Regulations.
(1) In accordance with the general
regulations in section 165.23 of this
part, entry into, transiting, or anchoring
within this safety zone is prohibited
unless authorized by the Captain of the
Port, Sector Lake Michigan or his
designated on-scene representative.
(2) This safety zone is closed to all
vessel traffic, except as may be
permitted by the Captain of the Port,
Sector Lake Michigan or his designated
on-scene representative.
(3) The ‘‘on-scene representative’’ of
the Captain of the Port, Sector Lake
Michigan is any Coast Guard
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42 CFR Part 84
[Docket No. CDC–2012–0009; NIOSH–258]
Self-Contained Breathing Apparatus
Remaining Service-Life Indicator
Performance Requirements
Centers for Disease Control and
Prevention, HHS.
ACTION: Final rule.
allows the manufacturer to offer
remaining service life set point at a
higher value or values appropriate to the
purchaser’s use scenario.
This final rule is effective
February 13, 2013.
DATES:
FOR FURTHER INFORMATION CONTACT:
Jonathan Szalajda, NIOSH National
Personal Protective Technology
Laboratory (NPPTL), P.O. Box 18070,
626 Cochrans Mill Road, Pittsburgh, PA
15236, (412) 386–5200 (this is not a tollfree number).
The
preamble to this final rule is organized
as follows:
SUPPLEMENTARY INFORMATION:
I. Public Participation
II. Background
III. Summary of Final Rule and Response to
Public Comments
IV. Regulatory Assessment Requirements
A. Executive Orders 12866 and 13563
B. Regulatory Flexibility Act
C. Paperwork Reduction Act
D. Small Business Regulatory Enforcement
Fairness Act
E. Unfunded Mandates Reform Act of 1995
F. Executive Order 12988 (Civil Justice)
G. Executive Order 13132 (Federalism)
H. Executive Order 13045 (Protection of
Children From Environmental Health
Risks and Safety Risks)
I. Executive Order 13211 (Actions
Concerning Regulations That
Significantly Affect Energy Supply,
Distribution, or Use)
J. Plain Writing Act of 2010
V. Final Rule
AGENCY:
On June 25, 2012, the
Department of Health and Human
Services (HHS) published a notice of
proposed rulemaking proposing to
update respirator approval standards in
response to a petition to amend our
regulations, current requirements for
self-contained breathing apparatus
(SCBA) remaining service-life indicators
or warning devices. These indicators are
built into a respirator to alert the user
that the breathing air provided by the
respirator is close to depletion. In this
final rule, HHS responds to public
comment on the proposed rule and
revises the current standard, employed
by the National Institute for
Occupational Safety and Health
(NIOSH) located within the Centers for
Disease Control and Prevention (CDC),
to allow greater flexibility in the setting
of the indicator alarm to ensure that the
alarm more effectively meets the
different worker protection needs of
different work operations. This final
rule sets a minimum alarm point at 25
percent of the rated service time and
SUMMARY:
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I. Public Participation
Interested persons or organizations
were invited to participate in this
rulemaking by submitting written views,
arguments, recommendations, and data.
Comments were invited on any topic
related to this proposal, but comments
were specifically solicited regarding
whether: (1) 25 percent of the rated
service time of the respirator is an
appropriate default setting for the
indicator to alarm; (2) the rule should
specify an upper limit that would
require that the indicator be set to alarm
no earlier than a set amount, such as 50
percent of rated service time; and (3)
there are possible emergency or rescue
scenarios for which one would want an
indicator to alarm at 50 percent or more
of the rated service time?
HHS received 8 submissions from the
public in response to this rulemaking.
Commenters represented local fire
departments, manufacturers of selfcontained breathing apparatus (SCBA)
used in the fire service, and a
firefighters’ union. A summary of
comments and the HHS response are
found in Section III, below.
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II. Background
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In 2003, NIOSH received a petition
from David Bernzweig of the Columbus
(OH) Professional Firefighters
International Association of Fire
Fighters (IAFF) Local 67 requesting that
the agency initiate rulemaking to amend
42 CFR 84.83(f).1 The current rule
requires that the self-contained
breathing apparatus (SCBA) service-life
indicator (also known in the firefighter
community as an end-of-service-time
indicator (EOSTI), or a low-air alarm)
give an alarm within the 20 to 25
percent range. Stakeholders in
agreement with Mr. Bernzweig
requested that HHS eliminate the lower
value (20 percent) and require the
indicator to alarm no later than at 25
percent of rated service time. NIOSH
considered the request and facilitated
discussion among stakeholders by
holding a public meeting to discuss
underlying issues and technical matters
on December 2, 2008, in Pittsburgh,
Pennsylvania (73 FR 65860, November
5, 2008).2
The National Fire Protection
Association (NFPA), which sets
standards for personal protective
equipment used in the fire service,
initiated an effort in 2008 to develop
consensus on the matter and recently
decided to amend NFPA 1981: Standard
on Open-Circuit Self-Contained
Breathing Apparatus (SCBA) for
Emergency Services 3 to require that the
indicator alarm at 33 percent.
For reasons discussed in the notice of
proposed rulemaking published in the
Federal Register on June 25, 2012 (77
FR 37862), HHS finds that amending
§ 84.83(f) to allow greater latitude with
regard to setting the indicator alarm
would not reduce the amount of
protection afforded to firefighters and
other SCBA users. In fact, HHS has
determined that specifying a minimum
setting of 25 percent and allowing
manufacturers to offer different alarm
settings more suited to purchasers’ use
scenarios will result in a more
1 National Institute for Occupational Safety and
Health, National Personal Protective Technology
Laboratory, transcript of public meeting held
December 2, 2008. Available at https://www.cdc.gov/
niosh/docket/archive/pdfs/NIOSH-034-A/0034-A120208-Transcript.pdf. Last accessed October 25,
2011.
2 The official transcript of this meeting as well as
public comments are available on NIOSH Docket
34–A (See https://www.cdc.gov/niosh/docket/
archive/docket034A.html). NIOSH had previously
collected public comments on remaining servicelife indicators in 2004 (See NIOSH Docket 34,
https://www.cdc.gov/niosh/docket/archive/
docket034.html).
3 NFPA 1981: Standard on open-circuit selfcontained breathing apparatus (SCBA) for
emergency services, Chapter 4. 2007 Edition.
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meaningful alarm that may offer greater
protection for users.
III. Summary of Final Rule and
Response to Public Comments
The amendment to 42 CFR 84.83(f)
establishes that the low-air indicator
must activate at a minimum setting of
25 percent of the SCBA’s rated service
time. If a purchaser has determined that
an earlier alarm will benefit the specific
occupational purpose for which the
respirator is to be used, the purchaser
may request that the manufacturer offer
a remaining service-life indicator alarm
set-point at a higher value (or values)
appropriate to the purchaser’s use
scenario. If the manufacturer chooses to
offer a respirator with a different setpoint (at no less than 25 percent of the
SCBA’s rated service time), the modified
respirator must be approved by NIOSH.
Purchasers may also have the indicator
setting modified for already fielded
SCBA units by an authorized
representative of the manufacturer,
provided that the respirator model has
received a new NIOSH approval
specifying the new alarm set-point.
The final rule also codifies a longstanding NIOSH policy requiring the
indicator for demand and pressuredemand open-circuit (OC)SCBA to
alarm continuously until the respirator’s
breathing air supply is depleted.
Changes to the proposed rule text are
made in response to public comment, to
clarify our overall intent; to specify that
the requirement for continuous alarming
is intended for open-circuit, demand
and pressure demand units only; and to
require that manufacturers identify the
indicator setting on each unit. Specific
comments and responses are discussed
below. The rule text is also amended
slightly to better comply with Federal
plain language requirements.
Comment: Two commenters were
fully supportive of the rulemaking. One
commenter stated that requiring fire
service respirators to alarm when
breathing air reaches 25 percent ‘‘does
not serve the needs or interests of
today’s fire service.’’ According to the
commenter, ‘‘[t]here is no safety
purpose served by not allowing an
earlier set point for the EOSTI. An
earlier set point would allow for a
greater margin of safety for the end user.
Not having an earlier set point would
continue to place firefighters at risk by
not having an adequate air reserve when
the EOSTI activates.’’ The commenter
further agreed that the alarm should not
be field-adjustable and that purchasers
should be able to specify the setting at
the time of purchase or service.
HHS response: We thank these
commenters for their response.
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Comment: We received two comments
that appeared to confuse the standard
proposed by HHS (a default of 25
percent unless the purchaser requests a
different, higher, value) with the
standard being developed by NFPA
(alarm activation at 33 percent). One
commenter expressed approval for
giving purchasers the ability to set the
remaining service-life indicator alarm
between 33 percent and 50 percent. The
other commenter expressed disapproval
for changing the indicator to activate at
33 percent rather than 25 percent.
HHS response: The amended standard
is responsive to the various concerns.
Manufacturers are not required to
modify existing approvals to comply
with this rule; they may continue to
market and sell respirators approved
under the current standard, indefinitely.
If, in response to purchaser needs, the
manufacturer chooses to market and sell
respirators that activate at the 25
percent minimum requirement or
earlier, the manufacturer must obtain a
new or revised NIOSH approval.
Comment: One commenter supported
the inclusion of a 50 percent upper limit
for the alarm set-point; other
commenters neither supported nor
opposed the upper limit.
HHS response: We did not receive
justification for applying a 50 percent
upper limit. It is conceivable that some
use scenarios might warrant an earlier
alarm point. Accordingly, we have not
revised the proposal in response to the
comment.
Comment: One commenter suggested
that allowing individual fire
departments to determine their own
remaining service-life indicator setting
may cause ‘‘incident related’’ problems.
The commenter further stated that there
was no discussion in the notice of
proposed rulemaking about the use of
the heads-up-display for monitoring
breathing air depletion or the reliance
on teamwork to maintain situational
awareness.
HHS response: This comment raises
training issues regarding the users’
response to an alarm being activated.
We understand that a change in the
mechanical alarm setting may
necessitate a change in training
protocols. However, training for the
proper use of these respirators is outside
the scope of this rulemaking.
Comment: One commenter agreed
with the intent of the proposed rule text
but suggested a number of edits. The
commenter stated that the proposed rule
text did not account for the distinction
between respirator models whose
alarms are designed either to activate
electronically or activate using the
device’s compressed air. According to
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the commenter, ‘‘[i]f the EOSTI is
activated electrically then the alarm can
sound continuously until the depletion
of the breathing air supply. If the EOSTI
is activated using the compressed air in
the system then at some point the alarm
sound will decrease in decibels and
even cease to sound before the breathing
air is depleted.’’ The commenter
suggested adding the text ‘‘if electrically
controlled or to a pressure of 10 bar (145
psi) if operated by the compressed air in
the system’’ to the text in § 84.83(f).
HHS response: The purpose of the
alarm is to advise the user that the
system is depleting its air supply. While
the rule text does not specifically
identify models that alarm either
electronically or using compressed air,
we intend for the indicator to alarm
until the air supply runs out in order to
warn the user of the situation so they
can take appropriate action for their
setting. That the indicator may not
continue to alarm until the air supply is
absolutely depleted is understood and is
evaluated in NIOSH testing (see NIOSH
standard testing procedure RCT–ASR–
STP–0124, Determination of Remaining
Service-Life Indicator—Open-Circuit,
Demand and Pressure-Demand, SelfContained Breathing Apparatus, at
https://www.cdc.gov/niosh/npptl/stps/
pdfs/RCT-ASR-0124.pdf, which will be
updated to comport with this
rulemaking).
Comment: Another comment referred
to long duration closed-circuit breathing
apparatus (CCBA), which are also
regulated under Subpart H in Part 84.
The commenter stated that ‘‘it can be
interpreted that even long duration
CCBA would also need to meet the
proposed new requirements. For
example, this would require that a
CCBA with a rated service time of 4
hours would need to have the EOSTI
alarm continuously for 1 hour and this
would be annoying to the users and may
affect their activities in a negative
manner.’’ The commenter accordingly
suggested that the text in § 84.83(f)
should address only open-circuit
devices, and offers a new § 84.83(g)
which suggests that, for closed-circuit
devices, the indicator should alarm for
a limited time period when the reserve
capacity of the apparatus is reached,
and a continuous alarm when a
prescribed pressure is reached.
HHS response: HHS did not intend for
the continuous alarm requirement to
pertain to long-duration closed-circuit
devices. However, the open-circuit
demand and pressure-demand devices
are expected to alarm continuously once
activated. Accordingly, we have
amended the final rule text to require
that only open-circuit demand and
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pressure-demand (as described in 42
CFR 84.70(a)(2)(i) and 42 CFR
84.70(a)(2)(ii)) respirators need to alarm
continuously.
Comment: One commenter suggested
that only purchasers who are required
by a third-party standard to request an
alarm set-point other than the default 25
percent be allowed to request a different
alarm setting.
HHS response: We do not agree that
the 25 percent default value should only
be raised when prescribed by a third
party standard. While § 84.83(f) is
amended in response to a petition on
behalf of the U.S. fire service, we note
that OC–SCBAs are used by industries
and in occupational settings other than
firefighting. We intend to maintain
flexibility with regard to the alarm
setting requirement to avoid further
limitations on the ability of purchasers
to request an alarm set-point
appropriate to their use scenarios and
the ability of manufacturers to offer
such respirators.
Comment: One commenter stated that
the terms ‘default’ and ‘adjusted’ used
in the rule summary are vague and
‘‘cause policy or test requirement
issues.’’ The commenter recommended
that the word ‘default’ be removed
because it ‘‘implies the product must
meet the minimum setting and shall be
capable of fulfilling a higher setting. We
believe this is not the intent of the
proposed changes and can lead to
unnecessarily design-restrictive
interpretations.’’ The commenter
requested that, in addition to adjustable
designs, the rule should ‘‘allow
flexibility to permit others such as
dedicated set point designs.’’ The
commenter suggested that the rule text
should be modified to state: ‘‘Each
remaining service-life indicator or
warning device shall give an alarm
when the remaining service life of the
apparatus is reduced to the
manufacturers’ specified range and shall
alarm continuously until the breathing
air supply approaches depletion. The
manufacturer can specify either a set
point of 25 or 33 percent of its rated
service time in response to the user’s
specific request.’’
HHS response: The terms ‘default’
and ‘adjusted’ do not occur in the rule
text; however, HHS does intend for the
product to be able to meet the 25
percent value as the minimum setting
and/or any higher setting requested by
the purchaser. During performance
testing for approval, NIOSH will test the
alarm setting identified by the
manufacturer in its request for approval
of the respirator system. If the
manufacturer does not identify an alarm
setting, the indicator will be tested to
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show that it activates at the value of 25
percent of its rated service life.
The rule does not specify or restrict
how manufacturers must comply with
its provisions; manufacturers who find
it in their best interest may offer specific
set-points. Manufacturers are not
required to produce a device that is
adjustable to different users’ needs, and
can continue to market and sell SCBA
models approved by NIOSH prior to the
effective date of this rule. However,
should the manufacturer wish to modify
such a model for any reason, including
a change to their service-life indicator
set point, the manufacturer is required
to apply to NIOSH for a new approval.
Additionally, in evaluating this
comment, HHS determined that the user
should be able to readily identify a
respirator’s alarm setting to distinguish
models from one another. Models that
meet the revised performance
requirements of this rule should have
labels and/or markings that identify the
alarm setting for that particular model.
At the discretion of the manufacturer,
these markings could be addressed as
part of the cautions and limitations
associated with these devices, or as an
additional label. In accordance with this
determination, the final rule text is
amended to address labels and/or
markings.
Comment: One commenter
recommended that 42 CFR 84.82
‘‘include an additional section for a 33
percent’’ remaining service-life
indicator. According to the commenter,
‘‘[a]llowing manufacturers the ability to
utilize the same gauge for both alarm set
points will reduce cost and complexity
within the market.’’
HHS response: HHS has determined
that the provisions in 42 CFR 84.82 are
sufficiently flexible to allow
manufacturers to produce gauges that
accurately indicate the amount of
breathing air contained in a unit.
Comment: HHS received one
comment on the E.O. 12866 and E.O.
13563 analysis in Section IV.A., below.
According to the commenter, ‘‘[i]t is
important to realize that additional costs
for multiple or adjustable set points are
inevitable. In addition to added design
and documentation costs, options
introduced into production will
increase assembly and inspection times.
Inventory costs increase with optional
material warehousing.* * *. While they
may be independent, other pressure
gauges and electronic systems must be
designed to correlate with the RSLI and
the system(s) must be thoroughly
verified. Differing RSLI settings may
require differing gauge faces and
electronics/programming designs to
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maintain correlation. For all these
reasons, costs will increase.’’
HHS response: The commenter
misunderstands the requirement. HHS
does not require manufacturers to
produce products with new features
allowing for adjustment of the service
life indicator alarm set point, or for
various product models with different
set points. Any manufacturer can
choose to meet product demand by
either manufacturing products with
fixed set points or by manufacturing
products with manufacturer-adjustable
set points. Alternatively, the
manufacturer can choose to take no
action, and continue to sell respirators
under existing NIOSH approvals. HHS
is reducing the longstanding constraint
on these product designs for a single
alarm set point. Accordingly, we
continue to conclude that there are no
costs associated with this rulemaking,
and solely benefits in terms of greater
flexibility for manufacturers to meet the
diverse needs of their customers.
IV. Regulatory Assessment
Requirements
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A. Executive Orders 12866 and 13563
Executive Orders 12866 and 13563
direct agencies to assess all costs and
benefits of available regulatory
alternatives and, if regulation is
necessary, to select regulatory
approaches that maximize net benefits
(including potential economic,
environmental, public health and safety
effects, distributive impacts, and
equity).
This final rule is not being treated as
a ‘‘significant’’ action under E.O. 12866.
It modifies the settings for an indicator
required by current regulation, as well
as codifies a long-standing policy of
requiring that the OC demand and
pressure demand SCBA indicator alarm
continuously once it has begun. The
current rule requires that a remaining
service-life indicator activate when the
breathing air provided by an OC
demand and pressure demand SCBA
reaches between 20 and 25 percent of its
rated limit. The final rule replaces the
range with a default value of 25 percent,
and allows manufacturers to offer
indicator set-point values at a higher
limit than 25 percent of remaining
breathing air.
All approved OC demand and
pressure demand SCBA models have a
remaining service-life indicator for
which alarm limits are set during
manufacturing. Allowing respirator
manufacturers to offer a respirator with
an earlier activation set-point value will
ensure that the alarm more effectively
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meets the varying worker protection
needs of different work operations.
Although HHS determined that there
are no costs and only benefits associated
with this rulemaking, we received one
comment on this economic analysis,
summarized above. As discussed above,
HHS continues to conclude that there
are no costs associated with this
rulemaking, and solely benefits in terms
of greater flexibility for manufacturers to
meet the diverse needs of their
customers.
The rule does not interfere with State,
local, or tribal governments in the
exercise of their governmental
functions.
B. Regulatory Flexibility Act
The Regulatory Flexibility Act (RFA),
5 U.S.C. 601 et seq., requires each
agency to consider the potential impact
of its regulations on small entities,
including small businesses, small
governmental units, and small not-forprofit organizations. As discussed
above, all OC demand and pressuredemand SCBA models are equipped
with a remaining service-life indicator
that will not require additional
expenditure of resources to set at the
activation limit. This final rule allows
small organizations such as local fire
departments to request an earlier
indicator activation set-point when
purchasing new devices from the
manufacturer. The Secretary of HHS has
certified to the Chief Counsel, Office of
Advocacy of the Small Business
Administration, that this rule does not
have a significant impact on a
substantial number of small entities.
Accordingly, no regulatory impact
analysis is required.
C. Paperwork Reduction Act of 1995
The Paperwork Reduction Act (PRA),
44 U.S.C. 3501 et seq., requires an
agency to invite public comment on and
to obtain OMB approval of any
regulation that requires 10 or more
people to report information to the
agency or to keep certain records. This
rule does not contain any information
collection requirements; thus HHS has
determined that the PRA does not apply
to this rule.
D. Small Business Regulatory
Enforcement Fairness Act
As required by Congress under the
Small Business Regulatory Enforcement
Fairness Act of 1996 (5 U.S.C. 801 et
seq.), HHS will report to Congress the
promulgation of a final rule, once it is
developed, prior to its taking effect. The
report will state that HHS has
concluded that the rule is not a ‘‘major
rule’’ because it is not likely to result in
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an annual effect on the economy of $100
million or more.
E. Unfunded Mandates Reform Act of
1995
Title II of the Unfunded Mandates
Reform Act of 1995 (2 U.S.C. 1531 et
seq.) directs agencies to assess the
effects of Federal regulatory actions on
State, local, and tribal governments, and
the private sector ‘‘other than to the
extent that such regulations incorporate
requirements specifically set forth in
law.’’ For purposes of the Unfunded
Mandates Reform Act, this final rule
does not include any Federal mandate
that may result in increased annual
expenditures in excess of $100 million
by state, local or tribal governments in
the aggregate, or by the private sector,
adjusted annually for inflation. For
2012, the inflation-adjusted threshold is
$139 million.
F. Executive Order 12988 (Civil Justice)
This final rule has been drafted and
reviewed in accordance with Executive
Order 12988, Civil Justice Reform, and
will not unduly burden the Federal
court system. The amendment to an
existing respirator approval standard
will apply uniformly to all applicants.
This final rule has been reviewed
carefully to eliminate drafting errors and
ambiguities.
G. Executive Order 13132 (Federalism)
HHS has reviewed this final rule in
accordance with Executive Order 13132
regarding federalism, and has
determined that it does not have
‘‘federalism implications.’’ The final
rule does not ‘‘have substantial direct
effects on the States, on the relationship
between the national government and
the States, or on the distribution of
power and responsibilities among the
various levels of government.’’
H. Executive Order 13045 (Protection of
Children From Environmental Health
Risks and Safety Risks)
In accordance with Executive Order
13045, HHS has evaluated the
environmental health and safety effects
of this final rule on children. HHS has
determined that the final rule will have
no effect on children.
I. Executive Order 13211 (Actions
Concerning Regulations That
Significantly Affect Energy Supply,
Distribution, or Use)
In accordance with Executive Order
13211, HHS has evaluated the effects of
this final rule on energy supply,
distribution, or use and has determined
that the rule will not have a significant
adverse effect.
E:\FR\FM\14JAR1.SGM
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2622
Federal Register / Vol. 78, No. 9 / Monday, January 14, 2013 / Rules and Regulations
J. Plain Writing Act of 2010
Under Public Law 111–274 (October
13, 2010), executive Departments and
Agencies are required to use plain
language in documents that explain to
the public how to comply with a
requirement the Federal Government
administers or enforces. HHS has
attempted to use plain language in
promulgating the final rule consistent
with the Federal Plain Writing Act
guidelines. HHS did not receive any
public comments on this matter.
V. Final Rule
Occupational safety and health,
Personal protective equipment,
Respirators.
Text of the Rule
For the reasons discussed in the
preamble, the Department of Health and
Human Services amends 42 CFR part 84
as follows:
PART 84—APPROVAL OF
RESPIRATORY PROTECTIVE DEVICES
1. The authority citation for part 84
continues to read as follows:
■
Authority: 29 U.S.C. 577a, 651 et seq., and
657(g); 30 U.S.C. 3, 5, 7, 811, 842(h), 844.
2. In § 84.83, revise paragraph (f) to
read as follows:
■
§ 84.83 Timers; elapsed time indicators;
remaining service life indicators; minimum
requirements.
*
*
*
*
(f) Each remaining service-life
indicator or warning device must give
an alarm when the remaining service
life is reduced to a minimum of 25
percent of its rated service time or any
higher minimum percent value or
values as specified in the approval.
Open-circuit demand and pressuredemand respirators must alarm
continuously until depletion of the
breathing air supply. The percent value
set for indicator activation must be
identified by labels and/or markings on
each respirator unit.
srobinson on DSK4SPTVN1PROD with
Dated: December 28, 2012.
Kathleen Sebelius,
Secretary.
[FR Doc. 2013–00371 Filed 1–11–13; 8:45 am]
BILLING CODE 4163–18–P
VerDate Mar<15>2010
16:17 Jan 11, 2013
Jkt 229001
Federal Emergency Management
Agency
44 CFR Part 64
[Docket ID FEMA–2012–0003; Internal
Agency Docket No. FEMA–8265]
Suspension of Community Eligibility
Federal Emergency
Management Agency, DHS.
ACTION: Final rule.
AGENCY:
This rule identifies
communities where the sale of flood
insurance has been authorized under
the National Flood Insurance Program
(NFIP) that are scheduled for
suspension on the effective dates listed
within this rule because of
noncompliance with the floodplain
management requirements of the
program. If the Federal Emergency
Management Agency (FEMA) receives
documentation that the community has
adopted the required floodplain
management measures prior to the
effective suspension date given in this
rule, the suspension will not occur and
a notice of this will be provided by
publication in the Federal Register on a
subsequent date. Also, information
identifying the current participation
status of a community can be obtained
from FEMA’s Community Status Book
(CSB). The CSB is available at https://
www.fema.gov/fema/csb.shtm.
DATES: The effective date of each
community’s scheduled suspension is
the third date (‘‘Susp.’’) listed in the
third column of the following tables.
FOR FURTHER INFORMATION: If you want
to determine whether a particular
community was suspended on the
suspension date or for further
information, contact David Stearrett,
Federal Insurance and Mitigation
Administration, Federal Emergency
Management Agency, 500 C Street SW.,
Washington, DC 20472, (202) 646–2953.
SUPPLEMENTARY INFORMATION: The NFIP
enables property owners to purchase
Federal flood insurance that is not
otherwise generally available from
private insurers. In return, communities
agree to adopt and administer local
floodplain management measures aimed
at protecting lives and new construction
from future flooding. Section 1315 of
the National Flood Insurance Act of
1968, as amended, 42 U.S.C. 4022,
prohibits the sale of NFIP flood
insurance unless an appropriate public
body adopts adequate floodplain
management measures with effective
SUMMARY:
List of Subjects in 42 CFR Part 84
*
DEPARTMENT OF HOMELAND
SECURITY
PO 00000
Frm 00008
Fmt 4700
Sfmt 4700
enforcement measures. The
communities listed in this document no
longer meet that statutory requirement
for compliance with program
regulations, 44 CFR part 59.
Accordingly, the communities will be
suspended on the effective date in the
third column. As of that date, flood
insurance will no longer be available in
the community. We recognize that some
of these communities may adopt and
submit the required documentation of
legally enforceable floodplain
management measures after this rule is
published but prior to the actual
suspension date. These communities
will not be suspended and will continue
to be eligible for the sale of NFIP flood
insurance. A notice withdrawing the
suspension of such communities will be
published in the Federal Register.
In addition, FEMA publishes a Flood
Insurance Rate Map (FIRM) that
identifies the Special Flood Hazard
Areas (SFHAs) in these communities.
The date of the FIRM, if one has been
published, is indicated in the fourth
column of the table. No direct Federal
financial assistance (except assistance
pursuant to the Robert T. Stafford
Disaster Relief and Emergency
Assistance Act not in connection with a
flood) may be provided for construction
or acquisition of buildings in identified
SFHAs for communities not
participating in the NFIP and identified
for more than a year on FEMA’s initial
FIRM for the community as having
flood-prone areas (section 202(a) of the
Flood Disaster Protection Act of 1973,
42 U.S.C. 4106(a), as amended). This
prohibition against certain types of
Federal assistance becomes effective for
the communities listed on the date
shown in the last column. The
Administrator finds that notice and
public comment procedures under 5
U.S.C. 553(b), are impracticable and
unnecessary because communities listed
in this final rule have been adequately
notified.
Each community receives 6-month,
90-day, and 30-day notification letters
addressed to the Chief Executive Officer
stating that the community will be
suspended unless the required
floodplain management measures are
met prior to the effective suspension
date. Since these notifications were
made, this final rule may take effect
within less than 30 days.
National Environmental Policy Act.
This rule is categorically excluded from
the requirements of 44 CFR part 10,
Environmental Considerations. No
environmental impact assessment has
been prepared.
Regulatory Flexibility Act. The
Administrator has determined that this
E:\FR\FM\14JAR1.SGM
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Agencies
[Federal Register Volume 78, Number 9 (Monday, January 14, 2013)]
[Rules and Regulations]
[Pages 2618-2622]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-00371]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
42 CFR Part 84
[Docket No. CDC-2012-0009; NIOSH-258]
RIN 0920-AA38
Self-Contained Breathing Apparatus Remaining Service-Life
Indicator Performance Requirements
AGENCY: Centers for Disease Control and Prevention, HHS.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: On June 25, 2012, the Department of Health and Human Services
(HHS) published a notice of proposed rulemaking proposing to update
respirator approval standards in response to a petition to amend our
regulations, current requirements for self-contained breathing
apparatus (SCBA) remaining service-life indicators or warning devices.
These indicators are built into a respirator to alert the user that the
breathing air provided by the respirator is close to depletion. In this
final rule, HHS responds to public comment on the proposed rule and
revises the current standard, employed by the National Institute for
Occupational Safety and Health (NIOSH) located within the Centers for
Disease Control and Prevention (CDC), to allow greater flexibility in
the setting of the indicator alarm to ensure that the alarm more
effectively meets the different worker protection needs of different
work operations. This final rule sets a minimum alarm point at 25
percent of the rated service time and allows the manufacturer to offer
remaining service life set point at a higher value or values
appropriate to the purchaser's use scenario.
DATES: This final rule is effective February 13, 2013.
FOR FURTHER INFORMATION CONTACT: Jonathan Szalajda, NIOSH National
Personal Protective Technology Laboratory (NPPTL), P.O. Box 18070, 626
Cochrans Mill Road, Pittsburgh, PA 15236, (412) 386-5200 (this is not a
toll-free number).
SUPPLEMENTARY INFORMATION: The preamble to this final rule is organized
as follows:
I. Public Participation
II. Background
III. Summary of Final Rule and Response to Public Comments
IV. Regulatory Assessment Requirements
A. Executive Orders 12866 and 13563
B. Regulatory Flexibility Act
C. Paperwork Reduction Act
D. Small Business Regulatory Enforcement Fairness Act
E. Unfunded Mandates Reform Act of 1995
F. Executive Order 12988 (Civil Justice)
G. Executive Order 13132 (Federalism)
H. Executive Order 13045 (Protection of Children From
Environmental Health Risks and Safety Risks)
I. Executive Order 13211 (Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution, or Use)
J. Plain Writing Act of 2010
V. Final Rule
I. Public Participation
Interested persons or organizations were invited to participate in
this rulemaking by submitting written views, arguments,
recommendations, and data. Comments were invited on any topic related
to this proposal, but comments were specifically solicited regarding
whether: (1) 25 percent of the rated service time of the respirator is
an appropriate default setting for the indicator to alarm; (2) the rule
should specify an upper limit that would require that the indicator be
set to alarm no earlier than a set amount, such as 50 percent of rated
service time; and (3) there are possible emergency or rescue scenarios
for which one would want an indicator to alarm at 50 percent or more of
the rated service time?
HHS received 8 submissions from the public in response to this
rulemaking. Commenters represented local fire departments,
manufacturers of self-contained breathing apparatus (SCBA) used in the
fire service, and a firefighters' union. A summary of comments and the
HHS response are found in Section III, below.
[[Page 2619]]
II. Background
In 2003, NIOSH received a petition from David Bernzweig of the
Columbus (OH) Professional Firefighters International Association of
Fire Fighters (IAFF) Local 67 requesting that the agency initiate
rulemaking to amend 42 CFR 84.83(f).\1\ The current rule requires that
the self-contained breathing apparatus (SCBA) service-life indicator
(also known in the firefighter community as an end-of-service-time
indicator (EOSTI), or a low-air alarm) give an alarm within the 20 to
25 percent range. Stakeholders in agreement with Mr. Bernzweig
requested that HHS eliminate the lower value (20 percent) and require
the indicator to alarm no later than at 25 percent of rated service
time. NIOSH considered the request and facilitated discussion among
stakeholders by holding a public meeting to discuss underlying issues
and technical matters on December 2, 2008, in Pittsburgh, Pennsylvania
(73 FR 65860, November 5, 2008).\2\
---------------------------------------------------------------------------
\1\ National Institute for Occupational Safety and Health,
National Personal Protective Technology Laboratory, transcript of
public meeting held December 2, 2008. Available at https://www.cdc.gov/niosh/docket/archive/pdfs/NIOSH-034-A/0034-A-120208-Transcript.pdf. Last accessed October 25, 2011.
\2\ The official transcript of this meeting as well as public
comments are available on NIOSH Docket 34-A (See https://www.cdc.gov/niosh/docket/archive/docket034A.html). NIOSH had previously
collected public comments on remaining service-life indicators in
2004 (See NIOSH Docket 34, https://www.cdc.gov/niosh/docket/archive/docket034.html).
---------------------------------------------------------------------------
The National Fire Protection Association (NFPA), which sets
standards for personal protective equipment used in the fire service,
initiated an effort in 2008 to develop consensus on the matter and
recently decided to amend NFPA 1981: Standard on Open-Circuit Self-
Contained Breathing Apparatus (SCBA) for Emergency Services \3\ to
require that the indicator alarm at 33 percent.
---------------------------------------------------------------------------
\3\ NFPA 1981: Standard on open-circuit self-contained breathing
apparatus (SCBA) for emergency services, Chapter 4. 2007 Edition.
---------------------------------------------------------------------------
For reasons discussed in the notice of proposed rulemaking
published in the Federal Register on June 25, 2012 (77 FR 37862), HHS
finds that amending Sec. 84.83(f) to allow greater latitude with
regard to setting the indicator alarm would not reduce the amount of
protection afforded to firefighters and other SCBA users. In fact, HHS
has determined that specifying a minimum setting of 25 percent and
allowing manufacturers to offer different alarm settings more suited to
purchasers' use scenarios will result in a more meaningful alarm that
may offer greater protection for users.
III. Summary of Final Rule and Response to Public Comments
The amendment to 42 CFR 84.83(f) establishes that the low-air
indicator must activate at a minimum setting of 25 percent of the
SCBA's rated service time. If a purchaser has determined that an
earlier alarm will benefit the specific occupational purpose for which
the respirator is to be used, the purchaser may request that the
manufacturer offer a remaining service-life indicator alarm set-point
at a higher value (or values) appropriate to the purchaser's use
scenario. If the manufacturer chooses to offer a respirator with a
different set-point (at no less than 25 percent of the SCBA's rated
service time), the modified respirator must be approved by NIOSH.
Purchasers may also have the indicator setting modified for already
fielded SCBA units by an authorized representative of the manufacturer,
provided that the respirator model has received a new NIOSH approval
specifying the new alarm set-point.
The final rule also codifies a long-standing NIOSH policy requiring
the indicator for demand and pressure-demand open-circuit (OC)SCBA to
alarm continuously until the respirator's breathing air supply is
depleted.
Changes to the proposed rule text are made in response to public
comment, to clarify our overall intent; to specify that the requirement
for continuous alarming is intended for open-circuit, demand and
pressure demand units only; and to require that manufacturers identify
the indicator setting on each unit. Specific comments and responses are
discussed below. The rule text is also amended slightly to better
comply with Federal plain language requirements.
Comment: Two commenters were fully supportive of the rulemaking.
One commenter stated that requiring fire service respirators to alarm
when breathing air reaches 25 percent ``does not serve the needs or
interests of today's fire service.'' According to the commenter,
``[t]here is no safety purpose served by not allowing an earlier set
point for the EOSTI. An earlier set point would allow for a greater
margin of safety for the end user. Not having an earlier set point
would continue to place firefighters at risk by not having an adequate
air reserve when the EOSTI activates.'' The commenter further agreed
that the alarm should not be field-adjustable and that purchasers
should be able to specify the setting at the time of purchase or
service.
HHS response: We thank these commenters for their response.
Comment: We received two comments that appeared to confuse the
standard proposed by HHS (a default of 25 percent unless the purchaser
requests a different, higher, value) with the standard being developed
by NFPA (alarm activation at 33 percent). One commenter expressed
approval for giving purchasers the ability to set the remaining
service-life indicator alarm between 33 percent and 50 percent. The
other commenter expressed disapproval for changing the indicator to
activate at 33 percent rather than 25 percent.
HHS response: The amended standard is responsive to the various
concerns. Manufacturers are not required to modify existing approvals
to comply with this rule; they may continue to market and sell
respirators approved under the current standard, indefinitely. If, in
response to purchaser needs, the manufacturer chooses to market and
sell respirators that activate at the 25 percent minimum requirement or
earlier, the manufacturer must obtain a new or revised NIOSH approval.
Comment: One commenter supported the inclusion of a 50 percent
upper limit for the alarm set-point; other commenters neither supported
nor opposed the upper limit.
HHS response: We did not receive justification for applying a 50
percent upper limit. It is conceivable that some use scenarios might
warrant an earlier alarm point. Accordingly, we have not revised the
proposal in response to the comment.
Comment: One commenter suggested that allowing individual fire
departments to determine their own remaining service-life indicator
setting may cause ``incident related'' problems. The commenter further
stated that there was no discussion in the notice of proposed
rulemaking about the use of the heads-up-display for monitoring
breathing air depletion or the reliance on teamwork to maintain
situational awareness.
HHS response: This comment raises training issues regarding the
users' response to an alarm being activated. We understand that a
change in the mechanical alarm setting may necessitate a change in
training protocols. However, training for the proper use of these
respirators is outside the scope of this rulemaking.
Comment: One commenter agreed with the intent of the proposed rule
text but suggested a number of edits. The commenter stated that the
proposed rule text did not account for the distinction between
respirator models whose alarms are designed either to activate
electronically or activate using the device's compressed air. According
to
[[Page 2620]]
the commenter, ``[i]f the EOSTI is activated electrically then the
alarm can sound continuously until the depletion of the breathing air
supply. If the EOSTI is activated using the compressed air in the
system then at some point the alarm sound will decrease in decibels and
even cease to sound before the breathing air is depleted.'' The
commenter suggested adding the text ``if electrically controlled or to
a pressure of 10 bar (145 psi) if operated by the compressed air in the
system'' to the text in Sec. 84.83(f).
HHS response: The purpose of the alarm is to advise the user that
the system is depleting its air supply. While the rule text does not
specifically identify models that alarm either electronically or using
compressed air, we intend for the indicator to alarm until the air
supply runs out in order to warn the user of the situation so they can
take appropriate action for their setting. That the indicator may not
continue to alarm until the air supply is absolutely depleted is
understood and is evaluated in NIOSH testing (see NIOSH standard
testing procedure RCT-ASR-STP-0124, Determination of Remaining Service-
Life Indicator--Open-Circuit, Demand and Pressure-Demand, Self-
Contained Breathing Apparatus, at https://www.cdc.gov/niosh/npptl/stps/pdfs/RCT-ASR-0124.pdf, which will be updated to comport with this
rulemaking).
Comment: Another comment referred to long duration closed-circuit
breathing apparatus (CCBA), which are also regulated under Subpart H in
Part 84. The commenter stated that ``it can be interpreted that even
long duration CCBA would also need to meet the proposed new
requirements. For example, this would require that a CCBA with a rated
service time of 4 hours would need to have the EOSTI alarm continuously
for 1 hour and this would be annoying to the users and may affect their
activities in a negative manner.'' The commenter accordingly suggested
that the text in Sec. 84.83(f) should address only open-circuit
devices, and offers a new Sec. 84.83(g) which suggests that, for
closed-circuit devices, the indicator should alarm for a limited time
period when the reserve capacity of the apparatus is reached, and a
continuous alarm when a prescribed pressure is reached.
HHS response: HHS did not intend for the continuous alarm
requirement to pertain to long-duration closed-circuit devices.
However, the open-circuit demand and pressure-demand devices are
expected to alarm continuously once activated. Accordingly, we have
amended the final rule text to require that only open-circuit demand
and pressure-demand (as described in 42 CFR 84.70(a)(2)(i) and 42 CFR
84.70(a)(2)(ii)) respirators need to alarm continuously.
Comment: One commenter suggested that only purchasers who are
required by a third-party standard to request an alarm set-point other
than the default 25 percent be allowed to request a different alarm
setting.
HHS response: We do not agree that the 25 percent default value
should only be raised when prescribed by a third party standard. While
Sec. 84.83(f) is amended in response to a petition on behalf of the
U.S. fire service, we note that OC-SCBAs are used by industries and in
occupational settings other than firefighting. We intend to maintain
flexibility with regard to the alarm setting requirement to avoid
further limitations on the ability of purchasers to request an alarm
set-point appropriate to their use scenarios and the ability of
manufacturers to offer such respirators.
Comment: One commenter stated that the terms `default' and
`adjusted' used in the rule summary are vague and ``cause policy or
test requirement issues.'' The commenter recommended that the word
`default' be removed because it ``implies the product must meet the
minimum setting and shall be capable of fulfilling a higher setting. We
believe this is not the intent of the proposed changes and can lead to
unnecessarily design-restrictive interpretations.'' The commenter
requested that, in addition to adjustable designs, the rule should
``allow flexibility to permit others such as dedicated set point
designs.'' The commenter suggested that the rule text should be
modified to state: ``Each remaining service-life indicator or warning
device shall give an alarm when the remaining service life of the
apparatus is reduced to the manufacturers' specified range and shall
alarm continuously until the breathing air supply approaches depletion.
The manufacturer can specify either a set point of 25 or 33 percent of
its rated service time in response to the user's specific request.''
HHS response: The terms `default' and `adjusted' do not occur in
the rule text; however, HHS does intend for the product to be able to
meet the 25 percent value as the minimum setting and/or any higher
setting requested by the purchaser. During performance testing for
approval, NIOSH will test the alarm setting identified by the
manufacturer in its request for approval of the respirator system. If
the manufacturer does not identify an alarm setting, the indicator will
be tested to show that it activates at the value of 25 percent of its
rated service life.
The rule does not specify or restrict how manufacturers must comply
with its provisions; manufacturers who find it in their best interest
may offer specific set-points. Manufacturers are not required to
produce a device that is adjustable to different users' needs, and can
continue to market and sell SCBA models approved by NIOSH prior to the
effective date of this rule. However, should the manufacturer wish to
modify such a model for any reason, including a change to their
service-life indicator set point, the manufacturer is required to apply
to NIOSH for a new approval.
Additionally, in evaluating this comment, HHS determined that the
user should be able to readily identify a respirator's alarm setting to
distinguish models from one another. Models that meet the revised
performance requirements of this rule should have labels and/or
markings that identify the alarm setting for that particular model. At
the discretion of the manufacturer, these markings could be addressed
as part of the cautions and limitations associated with these devices,
or as an additional label. In accordance with this determination, the
final rule text is amended to address labels and/or markings.
Comment: One commenter recommended that 42 CFR 84.82 ``include an
additional section for a 33 percent'' remaining service-life indicator.
According to the commenter, ``[a]llowing manufacturers the ability to
utilize the same gauge for both alarm set points will reduce cost and
complexity within the market.''
HHS response: HHS has determined that the provisions in 42 CFR
84.82 are sufficiently flexible to allow manufacturers to produce
gauges that accurately indicate the amount of breathing air contained
in a unit.
Comment: HHS received one comment on the E.O. 12866 and E.O. 13563
analysis in Section IV.A., below. According to the commenter, ``[i]t is
important to realize that additional costs for multiple or adjustable
set points are inevitable. In addition to added design and
documentation costs, options introduced into production will increase
assembly and inspection times. Inventory costs increase with optional
material warehousing.* * *. While they may be independent, other
pressure gauges and electronic systems must be designed to correlate
with the RSLI and the system(s) must be thoroughly verified. Differing
RSLI settings may require differing gauge faces and electronics/
programming designs to
[[Page 2621]]
maintain correlation. For all these reasons, costs will increase.''
HHS response: The commenter misunderstands the requirement. HHS
does not require manufacturers to produce products with new features
allowing for adjustment of the service life indicator alarm set point,
or for various product models with different set points. Any
manufacturer can choose to meet product demand by either manufacturing
products with fixed set points or by manufacturing products with
manufacturer-adjustable set points. Alternatively, the manufacturer can
choose to take no action, and continue to sell respirators under
existing NIOSH approvals. HHS is reducing the longstanding constraint
on these product designs for a single alarm set point. Accordingly, we
continue to conclude that there are no costs associated with this
rulemaking, and solely benefits in terms of greater flexibility for
manufacturers to meet the diverse needs of their customers.
IV. Regulatory Assessment Requirements
A. Executive Orders 12866 and 13563
Executive Orders 12866 and 13563 direct agencies to assess all
costs and benefits of available regulatory alternatives and, if
regulation is necessary, to select regulatory approaches that maximize
net benefits (including potential economic, environmental, public
health and safety effects, distributive impacts, and equity).
This final rule is not being treated as a ``significant'' action
under E.O. 12866. It modifies the settings for an indicator required by
current regulation, as well as codifies a long-standing policy of
requiring that the OC demand and pressure demand SCBA indicator alarm
continuously once it has begun. The current rule requires that a
remaining service-life indicator activate when the breathing air
provided by an OC demand and pressure demand SCBA reaches between 20
and 25 percent of its rated limit. The final rule replaces the range
with a default value of 25 percent, and allows manufacturers to offer
indicator set-point values at a higher limit than 25 percent of
remaining breathing air.
All approved OC demand and pressure demand SCBA models have a
remaining service-life indicator for which alarm limits are set during
manufacturing. Allowing respirator manufacturers to offer a respirator
with an earlier activation set-point value will ensure that the alarm
more effectively meets the varying worker protection needs of different
work operations.
Although HHS determined that there are no costs and only benefits
associated with this rulemaking, we received one comment on this
economic analysis, summarized above. As discussed above, HHS continues
to conclude that there are no costs associated with this rulemaking,
and solely benefits in terms of greater flexibility for manufacturers
to meet the diverse needs of their customers.
The rule does not interfere with State, local, or tribal
governments in the exercise of their governmental functions.
B. Regulatory Flexibility Act
The Regulatory Flexibility Act (RFA), 5 U.S.C. 601 et seq.,
requires each agency to consider the potential impact of its
regulations on small entities, including small businesses, small
governmental units, and small not-for-profit organizations. As
discussed above, all OC demand and pressure-demand SCBA models are
equipped with a remaining service-life indicator that will not require
additional expenditure of resources to set at the activation limit.
This final rule allows small organizations such as local fire
departments to request an earlier indicator activation set-point when
purchasing new devices from the manufacturer. The Secretary of HHS has
certified to the Chief Counsel, Office of Advocacy of the Small
Business Administration, that this rule does not have a significant
impact on a substantial number of small entities. Accordingly, no
regulatory impact analysis is required.
C. Paperwork Reduction Act of 1995
The Paperwork Reduction Act (PRA), 44 U.S.C. 3501 et seq., requires
an agency to invite public comment on and to obtain OMB approval of any
regulation that requires 10 or more people to report information to the
agency or to keep certain records. This rule does not contain any
information collection requirements; thus HHS has determined that the
PRA does not apply to this rule.
D. Small Business Regulatory Enforcement Fairness Act
As required by Congress under the Small Business Regulatory
Enforcement Fairness Act of 1996 (5 U.S.C. 801 et seq.), HHS will
report to Congress the promulgation of a final rule, once it is
developed, prior to its taking effect. The report will state that HHS
has concluded that the rule is not a ``major rule'' because it is not
likely to result in an annual effect on the economy of $100 million or
more.
E. Unfunded Mandates Reform Act of 1995
Title II of the Unfunded Mandates Reform Act of 1995 (2 U.S.C. 1531
et seq.) directs agencies to assess the effects of Federal regulatory
actions on State, local, and tribal governments, and the private sector
``other than to the extent that such regulations incorporate
requirements specifically set forth in law.'' For purposes of the
Unfunded Mandates Reform Act, this final rule does not include any
Federal mandate that may result in increased annual expenditures in
excess of $100 million by state, local or tribal governments in the
aggregate, or by the private sector, adjusted annually for inflation.
For 2012, the inflation-adjusted threshold is $139 million.
F. Executive Order 12988 (Civil Justice)
This final rule has been drafted and reviewed in accordance with
Executive Order 12988, Civil Justice Reform, and will not unduly burden
the Federal court system. The amendment to an existing respirator
approval standard will apply uniformly to all applicants. This final
rule has been reviewed carefully to eliminate drafting errors and
ambiguities.
G. Executive Order 13132 (Federalism)
HHS has reviewed this final rule in accordance with Executive Order
13132 regarding federalism, and has determined that it does not have
``federalism implications.'' The final rule does not ``have substantial
direct effects on the States, on the relationship between the national
government and the States, or on the distribution of power and
responsibilities among the various levels of government.''
H. Executive Order 13045 (Protection of Children From Environmental
Health Risks and Safety Risks)
In accordance with Executive Order 13045, HHS has evaluated the
environmental health and safety effects of this final rule on children.
HHS has determined that the final rule will have no effect on children.
I. Executive Order 13211 (Actions Concerning Regulations That
Significantly Affect Energy Supply, Distribution, or Use)
In accordance with Executive Order 13211, HHS has evaluated the
effects of this final rule on energy supply, distribution, or use and
has determined that the rule will not have a significant adverse
effect.
[[Page 2622]]
J. Plain Writing Act of 2010
Under Public Law 111-274 (October 13, 2010), executive Departments
and Agencies are required to use plain language in documents that
explain to the public how to comply with a requirement the Federal
Government administers or enforces. HHS has attempted to use plain
language in promulgating the final rule consistent with the Federal
Plain Writing Act guidelines. HHS did not receive any public comments
on this matter.
V. Final Rule
List of Subjects in 42 CFR Part 84
Occupational safety and health, Personal protective equipment,
Respirators.
Text of the Rule
For the reasons discussed in the preamble, the Department of Health
and Human Services amends 42 CFR part 84 as follows:
PART 84--APPROVAL OF RESPIRATORY PROTECTIVE DEVICES
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1. The authority citation for part 84 continues to read as follows:
Authority: 29 U.S.C. 577a, 651 et seq., and 657(g); 30 U.S.C.
3, 5, 7, 811, 842(h), 844.
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2. In Sec. 84.83, revise paragraph (f) to read as follows:
Sec. 84.83 Timers; elapsed time indicators; remaining service life
indicators; minimum requirements.
* * * * *
(f) Each remaining service-life indicator or warning device must
give an alarm when the remaining service life is reduced to a minimum
of 25 percent of its rated service time or any higher minimum percent
value or values as specified in the approval. Open-circuit demand and
pressure-demand respirators must alarm continuously until depletion of
the breathing air supply. The percent value set for indicator
activation must be identified by labels and/or markings on each
respirator unit.
Dated: December 28, 2012.
Kathleen Sebelius,
Secretary.
[FR Doc. 2013-00371 Filed 1-11-13; 8:45 am]
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