[Federal Register Volume 68, Number 141 (Wednesday, July 23, 2003)]
[Notices]
[Page 43538]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 03-18689]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 2003D-0282]


Guidance for Industry and FDA Staff; Medical Device User Fee and 
Modernization Act of 2002, Validation Data in Premarket Notification 
Submissions [510(k)s] for Reprocessed Single-Use Medical Devices; 
Availability; Correction

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice; correction.

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SUMMARY: The Food and Drug Administration (FDA) is correcting a notice 
that appeared in the Federal Register of July 8, 2003 (68 FR 40679). 
The document announced the availability of a guidance entitled 
``Guidance for Industry and FDA Staff; Medical Device User Fee and 
Modernization Act of 2002, Validation Data in Premarket Notification 
Submissions [510(k)s] for Reprocessed Single-Use Medical Devices; 
Availability.'' The document published with the incorrect docket 
number. This document corrects that error.

FOR FURTHER INFORMATION CONTACT: Joyce A. Strong, Office of Policy and 
Planning (HF-27), Food and Drug Administration, 5600 Fishers Lane, 
Rockville, MD 20857, 301-827-7010.

SUPPLEMENTARY INFORMATION: In FR Doc. 03-17135, appearing on page 40679 
in the Federal Register of July 8, 2003, the following correction is 
made:
    1. On page 40679, in the first column, in the heading of the 
document, ``[Docket No. 2003D-0232]'' is corrected to read ``[Docket 
No. 2003D-0282]''.

    Dated: July 17, 2003.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. 03-18689 Filed 7-22-03; 8:45 am]
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