[Federal Register: March 29, 2002 (Volume 67, Number 61)]
[Notices]
[Page 15210]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr29mr02-79]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. 01N-0402]
Agency Information Collection Activities; Announcement of OMB
Approval; Medical Devices; Third-Party Premarket Submission Review and
Quality System Inspections Under United States/European Community
Mutual Recognition Agreement
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) is announcing that a
collection of information entitled ``Medical Devices; Third-Party
Premarket Submission Review and Quality System Inspections Under United
States/European Community Mutual Recognition Agreement'' 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 the Federal Register of January 14, 2002
(67 FR 1770), 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 0910-0378.
The approval expires on March 31, 2005. A copy of the supporting
statement for this information collection is available on the Internet
at http://www.fda.gov/ohrms/dockets.
Dated: March 22, 2002.
Margaret M. Dotzel,
Associate Commissioner for Policy.
[FR Doc. 02-7526 Filed 3-28-02; 8:45 am]
BILLING CODE 4160-01-S