[Federal Register: November 27, 1998 (Volume 63, Number 228)]
[Proposed Rules]               
[Page 65566]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr27no98-20]

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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: Proposed rule; correction.

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SUMMARY: The Food and Drug Administration (FDA) is correcting a 
proposed rule that appeared in the Federal Register of September 29, 
1998 (63 FR 51874). The document proposed to amend certain regulations 
governing establishment registration and device listing by domestic 
distributors. The document was published with an error. This document 
corrects that error.

FOR FURTHER INFORMATION CONTACT: Walter W. Morgenstern, Center for 
Devices and Radiological Health (HFZ-305), Food and Drug 
Administration, 2094 Gaither Rd., Rockville, MD 20857, 301-594-4699.

SUPPLEMENTARY INFORMATION: In FR Doc. 98-25797 appearing on page 51874 
in the Federal Register of September 29, 1998, the following correction 
is made:
     On page 51875, 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. 98-31570 Filed 11-25-98; 8:45 am]
BILLING CODE 4160-01-F