[Federal Register Volume 62, Number 250 (Wednesday, December 31, 1997)] [Notices] [Page 68292] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 97-34079] ======================================================================= ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES The Office of the Secretary Information Collection Activity Under Emergency Review by the Office of Management and Budget (OMB) Title: Correction Notice for Survey of Biomedical Equipment Manufacturers for Year 2000 Compliance Correction On December 22, 1997 the Department of Health and Human Services published a document in the Federal Register concerning the survey of biomedical equipment manufacturers for Year 2000 compliance. It is located on page 62 FR 66869. The fourth sentence of the first full paragraph of the second column is incorrect. It reads ``Also, section 518 of the Food, Drug and Cosmetic Act requires notification of users or purchasers when a device presents a reasonable risk of substantial harm to public health.'' The sentence should read ``Also, section 518 of the Food, Drug and Cosmetic Act requires notification of users and purchasers when a device presents an unreasonable risk of substantial harm to public health.'' Dated: December 23, 1997. Tom Joyce, Reports Clearance Officer. [FR Doc. 97-34079 Filed 12-30-97; 8:45 am] BILLING CODE 4150-04-M