Agency information collection activities: Reporting and recordkeeping requirements,

[Federal Register: February 9, 1999 (Volume 64, Number 26)]

[Notices]

[Page 6365]

From the Federal Register Online via GPO Access [wais.access.gpo.gov]

[DOCID:fr09fe99-92]

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 98N-0394]

Agency Information Collection Activities; Announcement of OMB Approval; Medical Devices; Investigational Device Exemptions

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; Investigational Device Exemptions'' 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 November 23, 1998 (63 FR 64617), 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 0910-391. The approval expires on January 31, 2002. A copy of the supporting statement for this information collection is available on the Internet at ``http://www.fda.gov/ohrms/dockets''.

Dated: February 2, 1999. William K. Hubbard, Associate Commissioner for Policy Coordination.

[FR Doc. 99-3016Filed2-8-99; 8:45 am]

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