[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]



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.


SUMMARY: The Food and Drug Administration (FDA) is correcting a direct 
final rule that appeared in the

[[Page 65555]]

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]