Medical Diagnostic Equipment Accessibility Standards Advisory Committee, 67595-67596 [2012-27516]
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Federal Register / Vol. 77, No. 219 / Tuesday, November 13, 2012 / Proposed Rules
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List of Subjects in 19 CFR Part 360
Administrative practice and
procedure, Business and industry,
Imports, Reporting and recordkeeping
requirements, Steel.
For reasons discussed in the
preamble, we propose amending 19 CFR
360 as follows:
PART 360—STEEL IMPORT
MONITORING AND ANALYSIS SYSTEM
1. The authority citation for part 360
continues to read as follows:
Authority: 13 U.S.C. 301(a) and 302.
2. Section 360.105 is revised to read
as follows.
srobinson on DSK4SPTVN1PROD with
§ 360.105 Duration of the steel import
licensing requirement.
The licensing program will be in
effect through March 21, 2017, but may
be extended upon review and
notification in the Federal Register
prior to this expiration date. Licenses
will be required for all subject imports
entered during this period, even if the
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16:23 Nov 09, 2012
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entry summary documents are not filed
until after the expiration of this
program. The licenses will be valid for
10 business days after the expiration of
this program to allow for the final filing
of required Customs documentation.
Dated: November 2, 2012.
Francisco J. Sanchez,
Under Secretary for International Trade.
[FR Doc. 2012–27539 Filed 11–9–12; 8:45 am]
BILLING CODE 3510–DS–P
ARCHITECTURAL AND
TRANSPORTATION BARRIERS
COMPLIANCE BOARD
36 CFR Part 1195
[Docket No. ATBCB–2012–0003]
RIN 3014–AA40
Medical Diagnostic Equipment
Accessibility Standards Advisory
Committee
Architectural and
Transportation Barriers Compliance
Board.
ACTION: Notice of advisory committee
meeting.
AGENCY:
The Medical Diagnostic
Equipment Accessibility Standards
Advisory Committee (Committee) will
hold its second meeting. The second
Committee meeting was originally
planned for October 29 and 30, 2012 but
cancelled on these dates due to the
imminent approach of Hurricane Sandy.
On July 5, 2012, the Architectural and
Transportation Barriers Compliance
Board (Access Board) established an
advisory committee to make
recommendations to the Board on
matters associated with comments
received and responses to questions
included in a previously published
Notice of Proposed Rulemaking (NPRM)
on Medical Diagnostic Equipment
Accessibility Standards.
DATES: The Committee will meet on
December 3, 2012, from 10:00 a.m. to
5:00 p.m. and on December 4, 2012,
from 9:00 a.m. to 3:00 p.m.
ADDRESSES: The meeting will be held at
the Access Board’s Conference Room,
1331 F Street NW., Suite 800,
Washington, DC 20004–1111.
FOR FURTHER INFORMATION CONTACT: Rex
Pace, Office of Technical and
Information Services, Architectural and
Transportation Barriers Compliance
Board, 1331 F Street NW., Suite 1000,
Washington, DC 20004–1111.
Telephone number (202) 272–0023
(Voice); (202) 272–0052 (TTY).
SUMMARY:
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67595
Electronic mail address: pace@accessboard.gov.
On July 5,
2012, the Architectural and
Transportation Barriers Compliance
Board (Access Board) established an
advisory committee to make
recommendations to the Board on
matters associated with comments
received and responses to questions
included in a previously published
NPRM on Medical Diagnostic
Equipment Accessibility Standards. See
77 FR 6916 (February 9, 2012). The
NPRM and information related to the
proposed standards are available on the
Access Board’s Web site at: https://
www.access-board.gov/medicalequipment.htm.
The advisory committee will hold its
second meeting on December 3 and 4,
2012. The agenda for the meeting is
based on the one originally planned for
the October 29 and 30, 2012 meeting
dates that were cancelled because of
Hurricane Sandy. The agenda includes
the following:
• Review of previous committee
work;
• Formation of subcommittees based
on medical diagnostic equipment type;
• Presentation on the proposed
transfer surface size and anthropometric
data of people who use wheeled
mobility devices by Edward Steinfeld,
Arch. D., AIA, Director of the Center for
Inclusive Design and Environmental
Access;
• Continued discussion on transfer
surface height and size;
• Review and discussion on
permitted obstructions to the transfer
surface;
• Consideration of and possible
discussion on issues proposed by
committee members; and
• Discussion of administrative issues.
The preliminary meeting agenda,
along with information about the
committee, is available at the Access
Board’s Web site (https://www.accessboard.gov/medical-equipment.htm).
Committee meetings are open to the
public and interested persons can attend
the meetings and communicate their
views. Members of the public will have
opportunities to address the committee
on issues of interest to them during
public comment periods scheduled on
each day of the meeting.
The meetings will be accessible to
persons with disabilities. An assistive
listening system, computer assisted realtime transcription (CART), and sign
language interpreters will be provided.
Persons attending the meetings are
requested to refrain from using perfume,
cologne, and other fragrances for the
SUPPLEMENTARY INFORMATION:
E:\FR\FM\13NOP1.SGM
13NOP1
67596
Federal Register / Vol. 77, No. 219 / Tuesday, November 13, 2012 / Proposed Rules
comfort of other participants (see
www.access-board.gov/about/policies/
fragrance.htm for more information).
Also, persons wishing to provide
handouts or other written information to
the committee are requested to provide
electronic formats to Rex Pace via email
prior to the meetings so that alternate
formats can be distributed to committee
members.
David M. Capozzi,
Executive Director.
[FR Doc. 2012–27516 Filed 11–9–12; 8:45 am]
BILLING CODE 8150–01–P
ENVIRONMENTAL PROTECTION
AGENCY
40 CFR Part 52
[EPA–R08–OAR–2012–0846; FRL-9751–5]
Approval and Promulgation of Air
Quality Implementation Plans;
Montana; Revisions to the
Administrative Rules of Montana—Air
Quality, Subchapter 7, Subchapter 16
and Subchapter 17
Environmental Protection
Agency (EPA).
ACTION: Proposed rule.
AGENCY:
EPA is proposing to approve
new rules and revisions as submitted by
the State of Montana on September 23,
2011, as revisions to Montana’s State
Implementation Plan. Montana adopted
these rules on December 2, 2005, and
March 23, 2006. The new rules adopted
on December 2, 2005, became stateeffective on January 1, 2006; the new
rules and revisions adopted on March
23, 2006, became state-effective on April
7, 2006. These new rules and revisions
meet the requirements of the Clean Air
Act and EPA’s minor new source review
regulations. The intended effect of this
action is to propose to approve these
rules as they are consistent with the
Clean Air Act. This action is being taken
under section 110 of the Clean Air Act.
DATES: Comments must be received on
or before December 13, 2012.
ADDRESSES: Submit your comments,
identified by Docket ID No. EPA–R08–
OAR–2012–0846, by one of the
following methods:
• www.regulations.gov. Follow the
on-line instructions for submitting
comments.
• Email: daly.carl@epa.gov and
leone.kevin@epa.gov
• Fax: (303) 312–6064 (please alert
the individual listed in the FOR FURTHER
INFORMATION CONTACT if you are faxing
comments).
srobinson on DSK4SPTVN1PROD with
SUMMARY:
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• Mail: Carl Daly, Director, Air
Program, Environmental Protection
Agency (EPA), Region 8, Mailcode 8P–
AR, 1595 Wynkoop Street, Denver,
Colorado 80202–1129.
• Hand Delivery: Carl Daly, Director,
Air Program, Environmental Protection
Agency (EPA), Region 8, Mailcode 8P–
AR, 1595 Wynkoop Street, Denver,
Colorado 80202–1129. Such deliveries
are only accepted Monday through
Friday, 8:00 a.m. to 4:30 p.m., excluding
Federal holidays. Special arrangements
should be made for deliveries of boxed
information.
Instructions: Direct your comments to
Docket ID No. EPA–R08–OAR–2012–
0846. EPA’s policy is that all comments
received will be included in the public
docket without change and may be
made available online at
www.regulations.gov, including any
personal information provided, unless
the comment includes information
claimed to be Confidential Business
Information (CBI) or other information
whose disclosure is restricted by statute.
Do not submit information that you
consider to be CBI or otherwise
protected through www.regulations.gov
or email. The www.regulations.gov web
site is an ‘‘anonymous access’’ system,
which means EPA will not know your
identity or contact information unless
you provide it in the body of your
comment. If you send an email
comment directly to EPA, without going
through www.regulations.gov, your
email address will be automatically
captured and included as part of the
comment that is placed in the public
docket and made available on the
Internet. If you submit an electronic
comment, EPA recommends that you
include your name and other contact
information in the body of your
comment and with any disk or CD–ROM
you submit. If EPA cannot read your
comment due to technical difficulties
and cannot contact you for clarification,
EPA may not be able to consider your
comment. Electronic files should avoid
the use of special characters, any form
of encryption, and be free of any defects
or viruses. For additional information
about EPA’s public docket visit the EPA
Docket Center homepage at https://
www.epa.gov/epahome/dockets.htm.
For additional instructions on
submitting comments, go to Section I.
General Information of the
SUPPLEMENTARY INFORMATION section of
this document.
Docket: All documents in the docket
are listed in the www.regulations.gov
index. Although listed in the index,
some information is not publicly
available, e.g., CBI or other information
whose disclosure is restricted by statute.
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Certain other material, such as
copyrighted material, will be publicly
available only in hard copy. Publiclyavailable docket materials are available
either electronically in
www.regulations.gov or in hard copy at
the Air Program, Environmental
Protection Agency (EPA), Region 8,
1595 Wynkoop Street, Denver, Colorado
80202–1129. EPA requests that if at all
possible, you contact the individual
listed in the FOR FURTHER INFORMATION
CONTACT section to view the hard copy
of the docket. You may view the hard
copy of the docket Monday through
Friday, 8:00 a.m. to 4:00 p.m., excluding
Federal holidays.
FOR FURTHER INFORMATION CONTACT:
Kevin Leone, Air Program, Mailcode
8P–AR, Environmental Protection
Agency, Region 8, 1595 Wynkoop
Street, Denver, Colorado 80202–1129,
(303) 312–6227, or leone.kevin@epa.gov.
SUPPLEMENTARY INFORMATION:
Table of Contents
I. General Information
II. What is being addressed in this proposed
action?
III. What Authorities Apply to EPA’s
Proposed Action
IV. EPA’s Review and Proposed Action on
SIP Revisions
V. Summary of EPA’s Proposed Action
VI. Statutory and Executive Order Reviews
Definitions
For the purpose of this document, we
are giving meaning to certain words or
initials as follows:
(i) The words or initials Act or CAA
mean or refer to the Clean Air Act,
unless the context indicates otherwise.
(ii) The initials ARM mean or refer to
the Administrative Rule of Montana.
(iii) The words EPA, we, us or our
mean or refer to the United States
Environmental Protection Agency.
(iv) The initials MACT mean
Maximum Achievable Control
Technology.
(v) The initials MAQP mean Montana
Air Quality Permit.
(vi) The initials MRR mean
Monitoring, Reporting and
Recordkeeping.
(vii) The initials NAAQS mean
National Ambient Air Quality
Standards.
(viii) The initials NESHAP mean
National Emission Standards for
Hazardous Air Pollutants.
(ix) The initials NSR mean or refer to
new source review, a phrase intended to
encompass the stationary source
regulatory programs that regulate the
construction and modification of
stationary sources as provided under
CAA section 110(a)(2)(C), CAA Title I,
E:\FR\FM\13NOP1.SGM
13NOP1
Agencies
[Federal Register Volume 77, Number 219 (Tuesday, November 13, 2012)]
[Proposed Rules]
[Pages 67595-67596]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-27516]
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ARCHITECTURAL AND TRANSPORTATION BARRIERS COMPLIANCE BOARD
36 CFR Part 1195
[Docket No. ATBCB-2012-0003]
RIN 3014-AA40
Medical Diagnostic Equipment Accessibility Standards Advisory
Committee
AGENCY: Architectural and Transportation Barriers Compliance Board.
ACTION: Notice of advisory committee meeting.
-----------------------------------------------------------------------
SUMMARY: The Medical Diagnostic Equipment Accessibility Standards
Advisory Committee (Committee) will hold its second meeting. The second
Committee meeting was originally planned for October 29 and 30, 2012
but cancelled on these dates due to the imminent approach of Hurricane
Sandy. On July 5, 2012, the Architectural and Transportation Barriers
Compliance Board (Access Board) established an advisory committee to
make recommendations to the Board on matters associated with comments
received and responses to questions included in a previously published
Notice of Proposed Rulemaking (NPRM) on Medical Diagnostic Equipment
Accessibility Standards.
DATES: The Committee will meet on December 3, 2012, from 10:00 a.m. to
5:00 p.m. and on December 4, 2012, from 9:00 a.m. to 3:00 p.m.
ADDRESSES: The meeting will be held at the Access Board's Conference
Room, 1331 F Street NW., Suite 800, Washington, DC 20004-1111.
FOR FURTHER INFORMATION CONTACT: Rex Pace, Office of Technical and
Information Services, Architectural and Transportation Barriers
Compliance Board, 1331 F Street NW., Suite 1000, Washington, DC 20004-
1111. Telephone number (202) 272-0023 (Voice); (202) 272-0052 (TTY).
Electronic mail address: board.gov">pace@access-board.gov.
SUPPLEMENTARY INFORMATION: On July 5, 2012, the Architectural and
Transportation Barriers Compliance Board (Access Board) established an
advisory committee to make recommendations to the Board on matters
associated with comments received and responses to questions included
in a previously published NPRM on Medical Diagnostic Equipment
Accessibility Standards. See 77 FR 6916 (February 9, 2012). The NPRM
and information related to the proposed standards are available on the
Access Board's Web site at: https://www.access-board.gov/medical-equipment.htm.
The advisory committee will hold its second meeting on December 3
and 4, 2012. The agenda for the meeting is based on the one originally
planned for the October 29 and 30, 2012 meeting dates that were
cancelled because of Hurricane Sandy. The agenda includes the
following:
Review of previous committee work;
Formation of subcommittees based on medical diagnostic
equipment type;
Presentation on the proposed transfer surface
size and anthropometric data of people who use wheeled mobility devices
by Edward Steinfeld, Arch. D., AIA, Director of the Center for
Inclusive Design and Environmental Access;
Continued discussion on transfer surface height and size;
Review and discussion on permitted obstructions to the
transfer surface;
Consideration of and possible discussion on issues
proposed by committee members; and
Discussion of administrative issues.
The preliminary meeting agenda, along with information about the
committee, is available at the Access Board's Web site (https://www.access-board.gov/medical-equipment.htm).
Committee meetings are open to the public and interested persons
can attend the meetings and communicate their views. Members of the
public will have opportunities to address the committee on issues of
interest to them during public comment periods scheduled on each day of
the meeting.
The meetings will be accessible to persons with disabilities. An
assistive listening system, computer assisted real-time transcription
(CART), and sign language interpreters will be provided. Persons
attending the meetings are requested to refrain from using perfume,
cologne, and other fragrances for the
[[Page 67596]]
comfort of other participants (see www.access-board.gov/about/policies/fragrance.htm for more information). Also, persons wishing to provide
handouts or other written information to the committee are requested to
provide electronic formats to Rex Pace via email prior to the meetings
so that alternate formats can be distributed to committee members.
David M. Capozzi,
Executive Director.
[FR Doc. 2012-27516 Filed 11-9-12; 8:45 am]
BILLING CODE 8150-01-P