Advisory Committees; Filing of Closed Meeting Reports, 76357 [E8-29679]
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Federal Register / Vol. 73, No. 242 / Tuesday, December 16, 2008 / Notices
1. The staff memo to the Board will
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and the background material will be
made available on a computer disc in
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copy of the document, please call
Penelope Beattie on 202–452–3982.
2. This meeting will be recorded for
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copies can be ordered for $4 per disc by
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FOR FURTHER INFORMATION CONTACT:
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Skidmore, Assistant to the Board, Office
of Board Members at 202–452–2955.
SUPPLEMENTARY INFORMATION: You may
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announcement of this meeting; or you
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electronic announcement. (The Web site
also includes procedural and other
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Board of Governors of the Federal Reserve
System, December 11, 2008.
Robert deV. Frierson,
Deputy Secretary of the Board.
[FR Doc. E8–29823 Filed 12–12–08; 11:15
am]
BILLING CODE 6210–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2008–0038]
Advisory Committees; Filing of Closed
Meeting Reports
AGENCY:
Food and Drug Administration,
HHS.
sroberts on PROD1PC70 with NOTICES
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that, as required by the Federal
Advisory Committee Act, the agency has
filed with the Library of Congress the
annual reports of those FDA advisory
committees that held closed meetings
during fiscal year 2008.
ADDRESSES: Copies are available from
the Division of Dockets Management
(HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852, 301–827–
6860.
Management Officer, Advisory
Committee Oversight and Management
Staff (HF–4), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–827–1220.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Under
section 10(d) of the Federal Advisory
Committee Act (5 U.S.C. app.1) and 21
CFR 14.60(d), FDA has filed with the
Library of Congress the annual reports
for the following FDA advisory
committees that held closed meetings
during the period October 1, 2007,
through September 30, 2008:
Center for Biologics Evaluation and
Research:
Blood Products Advisory Committee,
Cellular, Tissue and Gene Therapies
Advisory Committee,
Vaccines and Related Biological
Products Advisory Committee,
Center for Drugs Evaluation and
Research:
Anesthetic and Life Support Drugs
Advisory Committee,
Oncologic Drugs Advisory Committee,
Center for Devices and Radiological
Health:
Medical Devices Advisory Committee
(consisting of reports for Circulatory
Drugs Devices Panel, Obstetrics and
Gynecology Devices Panel and the
Radiological Devices Panel),
National Center for Toxicological
Research:
Science Board to the National Center
for Toxicological Research.
Annual Reports are available for
public inspections between 9 a.m. and
4 p.m., Monday through Friday at the
following locations:
1. The Library of Congress, Madison
Bldg., Newspaper and Current
Periodical Reading Room, 101
Independence Ave. SE., rm. 133,
Washington, DC; and
2. The Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852.
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Medical Devices:
Humanitarian Use Devices
SUPPLEMENTARY INFORMATION:
Dated: December 9, 2008.
Randall W. Lutter,
Deputy Commissioner for Policy.
[FR Doc. E8–29679 Filed 12–15–08; 8:45 am]
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FOR FURTHER INFORMATION CONTACT:
Theresa L. Green, Committee
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Food and Drug Administration
[Docket No. FDA–2008–N–0512]
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: 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 January 15,
2009.
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:
202–395–6974, or e-mailed to
oiralsubmissions@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–0332. Also
include the FDA docket number found
in brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT:
Denver Presley, Jr., Office of Information
Management (HFA–710), Food and Drug
Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301–796–3793.
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.
Medical Devices: Humanitarian Use
Devices—21 CFR Part 814 (OMB
Control Number 0910–0332)—Extension
This collection of information
implements the humanitarian use
device (HUD) provision of section
520(m) of the Federal Food, Drug, and
Cosmetic Act (the act) (21 U.S.C.
360j(m)) and subpart H, part 814 (21
CFR part 814). Under section 520(m) of
the act, FDA is authorized to exempt a
HUD from the effectiveness
requirements of sections 514 and 515 of
the act (21 U.S.C. 360d and 360e)
provided that the device: (1) Is used to
treat or diagnose a disease or condition
that affects fewer than 4,000 individuals
in the United States; (2) would not be
E:\FR\FM\16DEN1.SGM
16DEN1
Agencies
[Federal Register Volume 73, Number 242 (Tuesday, December 16, 2008)]
[Notices]
[Page 76357]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-29679]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2008-0038]
Advisory Committees; Filing of Closed Meeting Reports
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing that, as
required by the Federal Advisory Committee Act, the agency has filed
with the Library of Congress the annual reports of those FDA advisory
committees that held closed meetings during fiscal year 2008.
ADDRESSES: Copies are available from the Division of Dockets Management
(HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061,
Rockville, MD 20852, 301-827-6860.
FOR FURTHER INFORMATION CONTACT: Theresa L. Green, Committee Management
Officer, Advisory Committee Oversight and Management Staff (HF-4), Food
and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-
827-1220.
SUPPLEMENTARY INFORMATION: Under section 10(d) of the Federal Advisory
Committee Act (5 U.S.C. app.1) and 21 CFR 14.60(d), FDA has filed with
the Library of Congress the annual reports for the following FDA
advisory committees that held closed meetings during the period October
1, 2007, through September 30, 2008:
Center for Biologics Evaluation and Research:
Blood Products Advisory Committee,
Cellular, Tissue and Gene Therapies Advisory Committee,
Vaccines and Related Biological Products Advisory Committee,
Center for Drugs Evaluation and Research:
Anesthetic and Life Support Drugs Advisory Committee,
Oncologic Drugs Advisory Committee,
Center for Devices and Radiological Health:
Medical Devices Advisory Committee (consisting of reports for
Circulatory Drugs Devices Panel, Obstetrics and Gynecology Devices
Panel and the Radiological Devices Panel),
National Center for Toxicological Research:
Science Board to the National Center for Toxicological Research.
Annual Reports are available for public inspections between 9 a.m.
and 4 p.m., Monday through Friday at the following locations:
1. The Library of Congress, Madison Bldg., Newspaper and Current
Periodical Reading Room, 101 Independence Ave. SE., rm. 133,
Washington, DC; and
2. The Division of Dockets Management (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
Dated: December 9, 2008.
Randall W. Lutter,
Deputy Commissioner for Policy.
[FR Doc. E8-29679 Filed 12-15-08; 8:45 am]
BILLING CODE 4160-01-S