[Federal Register Volume 68, Number 141 (Wednesday, July 23, 2003)] [Notices] [Page 43538] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 03-18689] ----------------------------------------------------------------------- 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] BILLING CODE 4160-01-S