Proposed Information Collection Activity; Comment Request, 20497-20498 [2015-08684]
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Federal Register / Vol. 80, No. 73 / Thursday, April 16, 2015 / Notices
PERSON TO CONTACT FOR INFORMATION:
Shawn Woodhead Werth,
Secretary and Clerk of the Commission.
[FR Doc. 2015–08906 Filed 4–14–15; 4:15 pm]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Judith Ingram, Press Officer, Telephone:
(202) 694–1220.
Administration for Children and
Families
[CDC–2014–0013; Docket Number NIOSH–
274]
BILLING CODE 6715–01–P
Issuance of Final Guidance Publication
FEDERAL RESERVE SYSTEM
National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC),
Department of Health and Human
Services (HHS).
AGENCY:
Notice of Proposals To Engage in or
To Acquire Companies Engaged in
Permissible Nonbanking Activities;
Correction
This notice corrects a notice (FR Doc.
2015–08045) published on pages 18442
and 18443 of the issue for Wednesday,
April 8, 2015.
Under the Federal Reserve Bank of
San Francisco heading, the entry for
Cathay Financial Holding Co., Ltd.,
Taipei, Taiwan, is revised to read as
follows:
A. Federal Reserve Bank of San
Francisco (Gerald C. Tsai, Director,
Applications and Enforcement) 101
Market Street, San Francisco, California
94105–1579:
1. Cathay Financial Holding Co., Ltd.,
Cathay Life Insurance Co., Ltd., Liang
Ting Industrial Co., Ltd., Lin Yuan
Investment Co., Ltd., Pai Hsing
Investment Co., Ltd., Tung Chi Capital
Co., Ltd., and Wan Ta Investment Co.,
Ltd., all in Taipei, Taiwan, and Wan
Bao Development Co., Ltd., New Taipei,
Taiwan; to acquire Conning Holdings
Corp., Hartford, Connecticut, and
thereby engage in financial and
investment advisory activities, and
agency transactional services for
customer investments, pursuant to
sections 225.28(b)(6) and (b)(7).
Comments on this application must
be received by April 23, 2015.
Board of Governors of the Federal Reserve
System, April 13, 2015.
Michael J. Lewandowski,
Associate Secretary of the Board.
Notice of issuance of final
guidance publication.
ACTION:
The National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC),
announces the availability of the
following publication: ‘‘NIOSH Current
Intelligence Bulletin 67: Promoting
Health and Preventing Disease and
Injury through Workplace Tobacco
Policies’’ [2015–113].
SUMMARY:
This document may be
obtained at the following link: https://
www.cdc.gov/niosh/docs/2015-113/.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Michelle Martin, NIOSH Division of
Respiratory Disease Studies, 1095
Willowdale Road, Mailstop H–2900,
Morgantown, WV 26505–2888. (304)
285–5734 (not a toll free number).
Dated: April 9, 2015.
John Howard,
Director, National Institute for Occupational
Safety and Health, Centers for Disease Control
and Prevention.
[FR Doc. 2015–08737 Filed 4–15–15; 8:45 am]
BILLING CODE 4163–19–P
[FR Doc. 2015–08713 Filed 4–15–15; 8:45 am]
BILLING CODE 6210–01–P
Proposed Information Collection
Activity; Comment Request
Proposed Projects: Immediate Disaster
Case Management Intake Assessment
(hardcopy and electronic versions).
Title: Immediate Disaster Case
Management Intake Assessment.
OMB No.: 0970–NEW.
Description: Section 426 of the Robert
T. Stafford Disaster Relief and
Emergency Assistance Act (Stafford
Act), as amended, 42 U.S.C. 5189d
authorizes the Federal Emergency
Management Agency (FEMA) and the
U.S. Department of Health Services’
Administration for Children and
Families (ACF) to provide Immediate
Disaster Case Management (IDCM)
services under the federal Disaster Case
Management Program (DCMP).
The use of the Electronic Case
Management Record System (ECMRS) is
aligned with Executive Order of the
President 13589 and the memorandum
to the Heads of Executive Departments
and Agencies M–12–12 from the Office
of Management and Budget to ‘‘Promote
Efficient Spending to Support Agency
Operations.’’
The primary purpose of the
information collection pertains to ACF/
OHSEPR’s initiative to improve the
intake process and delivery of case
management services to individuals and
households impacted by a disaster.
Further, the information collection will
be used to support ACF/OHSEPR’s goal
to quickly identify critical gaps,
resources, needs, and services to
support State, local and non-profit
capacity for disaster case management
and to augment and build capacity
where none exists. All information
gathered will be exclusively used to
inform the delivery of disaster case
management services and programmatic
strategies and improvements.
Respondents: Individuals impacted by
a disaster.
ANNUAL BURDEN ESTIMATES
tkelley on DSK3SPTVN1PROD with NOTICES
Instrument
Number of
respondents
Number of
responses per
respondent
Burden hours
per response
Total burden
hours
IDCM Intake Assessment ................................................................................
3,500
1
40
2,333
Estimated Total Annual Burden
Hours: 2,333 hours or 140,000 minutes
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Administration for Children and
Families is soliciting public comment
on the specific aspects of the
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20498
Federal Register / Vol. 80, No. 73 / Thursday, April 16, 2015 / Notices
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Planning, Research
and Evaluation, 370 L’Enfant
Promenade SW., Washington, DC 20447,
Attn: ACF Reports Clearance Officer.
Email address: infocollection@
acf.hhs.gov. All requests should be
identified by the title of the information
collection.
The Department specifically requests
comments on: (a) Whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2015–08684 Filed 4–15–15; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2011–N–0672]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Prominent and
Conspicuous Mark of Manufacturers
on Single-Use Devices
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by May 18,
2015.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–7285, or emailed to oira_
submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–0577. Also
include the FDA docket number found
in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT: FDA
PRA Staff, Office of Operations, Food
and Drug Administration, 8455
Colesville Rd., COLE–14526, Silver
Spring, MD 20993–0002, PRAStaff@
fda.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
SUMMARY:
Prominent and Conspicuous Mark of
Manufacturers On Single-Use Devices
(OMB Control Number 0910–0577)—
Extension
Section 502 of the Federal Food, Drug,
and Cosmetic Act (the FD&C Act) (21
U.S.C. 352), among other things,
establishes requirements that the label
or labeling of a medical device must
meet so that it is not misbranded and
subject to regulatory action. Section 301
of the Medical Device User Fee and
Modernization Act of 2002 (Pub. L. 107–
250) amended section 502 of the FD&C
Act to add section 502(u) to require
devices (both new and reprocessed) to
bear prominently and conspicuously the
name of the manufacturer, a generally
recognized abbreviation of such name,
or a unique and generally recognized
symbol identifying the manufacturer.
Section 2(c) of the Medical Device
User Fee Stabilization Act of 2005 (Pub.
L. 109–43) amends section 502(u) of the
FD&C Act by limiting the provision to
reprocessed single-use devices (SUDs)
and the manufacturers who reprocess
them. Under the amended provision, if
the original SUD or an attachment to it
prominently and conspicuously bears
the name of the manufacturer, then the
reprocessor of the SUD is required to
identify itself by name, abbreviation, or
symbol in a prominent and conspicuous
manner on the device or attachment to
the device. If the original SUD does not
prominently and conspicuously bear the
name of the manufacturer, the
manufacturer who reprocesses the SUD
for reuse may identify itself using a
detachable label that is intended to be
affixed to the patient record.
The requirements of section 502(u) of
the FD&C Act impose a minimal burden
on industry. This section of the FD&C
Act only requires the manufacturer,
packer, or distributor of a device to
include their name and address on the
labeling of a device. This information is
readily available to the establishment
and easily supplied. From its
registration and premarket submission
database, FDA estimates that there are
67 establishments that distribute
approximately 427 reprocessed SUDs.
Each response is anticipated to take 0.1
hours (6 minutes) resulting in a total
burden to industry of 43 hours.
In the Federal Register of December
30, 2014 (79 FR 78445), FDA published
a 60-day notice requesting public
comment on the proposed collection of
information. No comments were
received.
FDA estimates the burden of this
collection of information as follows:
TABLE 1—ESTIMATED ANNUAL THIRD-PARTY DISCLOSURE BURDEN 1 2
Number of
disclosures
per respondent
Number of
respondents
Type of respondent
Total annual
disclosures
Average
burden per
disclosure
Total hours
tkelley on DSK3SPTVN1PROD with NOTICES
Establishments listing fewer than 10 SUDs .......................
Establishments listing 10 or more SUDs ............................
58
9
2
34
116
306
0.1 (6 minutes)
0.1 (6 minutes)
12
31
Total .............................................................................
......................
............................
........................
.........................
43
1 There
are no capital costs or operating and maintenance costs associated with this collection of information.
have been rounded.
2 Numbers
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]]>Agencies
[Federal Register Volume 80, Number 73 (Thursday, April 16, 2015)]
[Notices]
[Pages 20497-20498]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-08684]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Projects: Immediate Disaster Case Management Intake
Assessment (hardcopy and electronic versions).
Title: Immediate Disaster Case Management Intake Assessment.
OMB No.: 0970-NEW.
Description: Section 426 of the Robert T. Stafford Disaster Relief
and Emergency Assistance Act (Stafford Act), as amended, 42 U.S.C.
5189d authorizes the Federal Emergency Management Agency (FEMA) and the
U.S. Department of Health Services' Administration for Children and
Families (ACF) to provide Immediate Disaster Case Management (IDCM)
services under the federal Disaster Case Management Program (DCMP).
The use of the Electronic Case Management Record System (ECMRS) is
aligned with Executive Order of the President 13589 and the memorandum
to the Heads of Executive Departments and Agencies M-12-12 from the
Office of Management and Budget to ``Promote Efficient Spending to
Support Agency Operations.''
The primary purpose of the information collection pertains to ACF/
OHSEPR's initiative to improve the intake process and delivery of case
management services to individuals and households impacted by a
disaster. Further, the information collection will be used to support
ACF/OHSEPR's goal to quickly identify critical gaps, resources, needs,
and services to support State, local and non-profit capacity for
disaster case management and to augment and build capacity where none
exists. All information gathered will be exclusively used to inform the
delivery of disaster case management services and programmatic
strategies and improvements.
Respondents: Individuals impacted by a disaster.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of
Instrument Number of responses per Burden hours Total burden
respondents respondent per response hours
----------------------------------------------------------------------------------------------------------------
IDCM Intake Assessment...................... 3,500 1 40 2,333
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 2,333 hours or 140,000 minutes
In compliance with the requirements of Section 506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Administration for Children and
Families is soliciting public comment on the specific aspects of the
[[Page 20498]]
information collection described above. Copies of the proposed
collection of information can be obtained and comments may be forwarded
by writing to the Administration for Children and Families, Office of
Planning, Research and Evaluation, 370 L'Enfant Promenade SW.,
Washington, DC 20447, Attn: ACF Reports Clearance Officer. Email
address: infocollection@acf.hhs.gov. All requests should be identified
by the title of the information collection.
The Department specifically requests comments on: (a) Whether the
proposed collection of information is necessary for the proper
performance of the functions of the agency, including whether the
information shall have practical utility; (b) the accuracy of the
agency's estimate of the burden of the proposed collection of
information; (c) the quality, utility, and clarity of the information
to be collected; and (d) ways to minimize the burden of the collection
of information on respondents, including through the use of automated
collection techniques or other forms of information technology.
Consideration will be given to comments and suggestions submitted
within 60 days of this publication.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2015-08684 Filed 4-15-15; 8:45 am]
BILLING CODE 4184-01-P
