[Federal Register Volume 63, Number 228 (Friday, November 27, 1998)] [Rules and Regulations] [Pages 65554-65555] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 98-31569] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Part 807 [Docket No. 98N-0520] Medical Devices; Establishment Registration and Device Listing for Manufacturers and Distributors of Devices; Correction
Agency
Food and Drug Administration, HHS.
Action
Direct final rule; correction.
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Summary
The Food and Drug Administration (FDA) is correcting a direct final rule that appeared in the
Federal Register of September 29, 1998 (63 FR 51825). The document amended certain regulations governing establishment registration and device listing by domestic distributors. The document was published with an error. This document corrects that error.
EFFECTIVE DATE: February 11, 1999.
For Further Information Contact
Walter W. Morgenstern, Center for Devices and Radiological Health (HFZ-305), Food and Drug Administration, 2094 Gaither Rd., Rockville, MD 20850, 301-594-4699.
Supplementary Information
In FR Docs. 98-25796 appearing on page 51825 in the Federal Register of September 29, 1998, the following correction is made: On page 51826, in the third column, amendatory paragraph four is corrected to read: 4. Section 807.20 is amended by revising paragraph (a)(4), by removing paragraph (c), by redesignating paragraph (d) as paragraph (c), and by adding paragraph (c)(3) to read as follows: * * * * *
Dated: November 19, 1998. William K. Hubbard, Associate Commissioner for Policy Coordination. [FR Doc. 98-31569 Filed 11-25-98; 8:45 am] BILLING CODE 4160-01-F