Agency information collection activities: Reporting and recordkeeping requirements,

[Federal Register: February 4, 1999 (Volume 64, Number 23)]

[Notices]

[Page 5665]

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

[DOCID:fr04fe99-65]

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 97N-0022]

Agency Information Collection Activities; Announcement of OMB Approval; Hearing Aid Devices: Professional and Patient Package Labeling and Conditions for Sale

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

SUMMARY: The Food and Drug Administration (FDA) is announcing that a collection of information entitled ``Hearing Aid Devices: Professional and Patient Package Labeling and Conditions for Sale'' 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 26, 1998 (63 FR 57127), 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 0910-0171. The approval expires on December 31, 1999. Copies of this document are available on the Internet at ``http://www.fda.gov/ohrms/dockets''.

Dated: January 27, 1999. William K. Hubbard, Associate Commissioner for Policy Coordination.

[FR Doc. 99-2685Filed2-3-99; 8:45 am]

BILLING CODE 4160-01-F