68 FR 141 pg. 43538 - 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
Type: NOTICEVolume: 68Number: 141Page: 43538
Docket number: [Docket No. 2003D-0282]
FR document: [FR Doc. 03-18689 Filed 7-22-03; 8:45 am]
Agency: Health and Human Services Department
Sub Agency: Food and Drug Administration
Official PDF Version: PDF Version
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.
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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