[Federal Register Volume 66, Number 140 (Friday, July 20, 2001)]
[Notices]
[Page 37976]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 01-18160]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 01N-0063]


Agency Information Collection Activities; Announcement of OMB 
Approval; Medical Devices; Current Good Manufacturing Practice (CGMP), 
Quality System (QS) Regulation

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The Food and Drug Administration (FDA) is announcing that a 
collection of information entitled ``Medical Devices; Current Good 
Manufacturing Practice (CGMP), Quality System (QS) Regulation'' has 
been approved by the Office of Management and Budget (OMB) under the 
Paperwork Reduction Act of 1995.

FOR FURTHER INFORMATION CONTACT: Peggy Schlosburg, Office of 
Information Resources Management (HFA-250), Food and Drug 
Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-827-1223.

SUPPLEMENTARY INFORMATION: In theFederal Register of May 31, 2001 (66 
FR 29577), the agency announced that the proposed information 
collection had been submitted to OMB for review and clearance under 44 
U.S.C. 3507. An agency may not conduct or sponsor, and a person is not 
required to respond to, a collection of information unless it displays 
a currently valid OMB control number. OMB has now approved the 
information collection and has assigned OMB control number 0910-0073. 
The approval expires on July 31, 2004. A copy of the supporting 
statement for this information collection is available on the Internet 
at http://www.fda.gov/ohrms/dockets.

    Dated: July 16, 2001.
Margaret M. Dotzel,
Associate Commissioner for Policy.
[FR Doc. 01-18160 Filed 7-19-01; 8:45 am]
BILLING CODE 4160-01-S