Advisory Committees; Filing of Closed Meeting Reports, 76357 [E8-29679]

Download as PDF Federal Register / Vol. 73, No. 242 / Tuesday, December 16, 2008 / Notices 1. The staff memo to the Board will be made available to the public in paper and the background material will be made available on a computer disc in Word format. If you require a paper copy of the document, please call Penelope Beattie on 202–452–3982. 2. This meeting will be recorded for the benefit of those unable to attend. Computer discs (CDs) will then be available for listening in the Board’s Freedom of Information Office, and copies can be ordered for $4 per disc by calling 202–452–3684 or by writing to: Freedom of Information Office, Board of Governors of the Federal Reserve System, Washington, D.C. 20551. FOR FURTHER INFORMATION CONTACT: Michelle Smith, Director, or Dave Skidmore, Assistant to the Board, Office of Board Members at 202–452–2955. SUPPLEMENTARY INFORMATION: You may call 202–452–3206 for a recorded announcement of this meeting; or you may contact the Board’s Web site at http://www.federalreserve.gov for an electronic announcement. (The Web site also includes procedural and other information about the open meeting.) 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] BILLING CODE 4160–01–S FOR FURTHER INFORMATION CONTACT: Theresa L. Green, Committee VerDate Aug<31>2005 17:09 Dec 15, 2008 Jkt 217001 76357 PO 00000 Frm 00028 Fmt 4703 Sfmt 4703 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.

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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