[Federal Register: February 4, 2003 (Volume 68, Number 23)]
[Notices]               
[Page 5643]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr04fe03-53]                         


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DEPARTMENT OF HEALTH AND HUMAN SERVICES


Food and Drug Administration


[Docket No. 02N-0355]


 
Agency Information Collection Activities; Announcement of OMB 
Approval; Medical Device Recall Authority


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 Device Recall Authority'' 
has been approved by the Office of Management and Budget (OMB) under 
the Paperwork Reduction Act of 1995.


FOR FURTHER INFORMATION CONTACT: Peggy Robbins, 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 November 13, 2002 
(67 FR 68876), 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 0910-0432. 
The approval expires on January 31, 2006. A copy of the supporting 
statement for this information collection is available on the Internet 
at http://www.fda.gov/ohrms/dockets.


    Dated: January 28, 2003.
Margaret M. Dotzel,
Assistant Commissioner for Policy.
[FR Doc. 03-2600 Filed 2-3-03; 8:45 am]

BILLING CODE 4160-01-S