[Federal Register: January 19, 1999 (Volume 64, Number 11)]
[Notices]               
[Page 2906-2907]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr19ja99-78]

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration
[Docket No. 98N-0331]

 
Agency Information Collection Activities; Announcement of OMB 
Approval; Medical Devices: Third-Party Review Program under FDAMA

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 
Review Program under FDAMA'' 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 October 30, 1998 
(63 FR 58397), the agency announced that

[[Page 2907]]

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 0910-0375. The approval expires on December 31, 2001.

    Dated: January 6, 1999.
William K. Hubbard,
Associate Commissioner for Policy Coordination.
[FR Doc. 99-1039 Filed 1-15-99; 8:45 am]
BILLING CODE 4160-01-F