[Federal Register Volume 59, Number 62 (Thursday, March 31, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-7629]


[[Page Unknown]]

[Federal Register: March 31, 1994]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES
21 CFR Part 821

[Docket No. 91N-0296]

 

Medical Devices; Illustrative and Designated Lists for Device 
Tracking; Correction

AGENCY: Food and Drug Administration, HHS.
ACTION: Final rule and request for comments; correction

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SUMMARY: The Food and Drug Administration (FDA) is correcting a final 
rule that appeared in the Federal Register of August 16, 1993 (58 FR 
43451), which amended the medical device tracking regulations to add 
the temporo-mandibular joint prostheses to the illustrative list of 
devices and the penile inflatable implant to the list of devices 
designated for tracking. The document was published with a 
typographical error. This document corrects that error.
EFFECTIVE DATE: August 29, 1993.
FOR FURTHER INFORMATION CONTACT: Joseph M. Sheehan, Center for Devices 
and Radiological Health (HFZ-84), Food and Drug Administration, 2098 
Gaither Rd., Rockville, MD 20850, 301-594-4765.
    In FR Doc. 93-19470, appearing on page 43451, in the Federal 
Register of Monday, August 16, 1993, the following correction is made:


Sec. 821.20  [Amended]

    On page 43455, in the 3d column, in amendatory instruction 2b. for 
Sec. 821.20, in line 5, ``878.5725'' is corrected to read ``880.5725''.

    Dated: March 25, 1994.
Michael R. Taylor,
Deputy Commissioner for Policy.
[FR Doc. 94-7629 Filed 3-30-94; 8:45 am]
BILLING CODE 4160-01-F