[Federal Register Volume 69, Number 89 (Friday, May 7, 2004)] [Rules and Regulations] [Page 25489] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 04-10265] [[Page 25489]] ======================================================================= ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Part 807 Medical Device Reports; Reports of Corrections and Removals; Establishment Registration and Device Listing: Premarket Approval Supplements; Quality System Regulation; Importation of Electronic Products; Technical Amendment; Correction AGENCY: Food and Drug Administration, HHS. ACTION: Final rule; technical amendment; correction. ----------------------------------------------------------------------- SUMMARY: The Food and Drug Administration (FDA) is correcting a final rule that appeared in the Federal Register of April 8, 2004 (69 FR 18472). That document corrected a final rule that appeared in the Federal Register of March 10, 2004 (69 FR 11310). The April 8, 2004, document published with inadvertent errors. This document corrects those errors. DATES: This rule is effective May 7, 2004. 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. 04-8022, appearing on page 18472 in the Federal Register of Thursday, April 8, 2004, the following corrections are made: 1. On page 18472, in the third column, under the FOR FURTHER INFORMATION CONTACT heading, the address is corrected to read ``Joyce A. Strong, Office of Policy and Planning (HF-27), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-827-7010.'' Sec. 807.22 [Corrected] 2. On page 18473, in the first column, in Sec. 807.22, in paragraph (a), the first sentence is corrected to read ``The first registration of a device establishment shall be on Form FDA-2891 (Initial Registration of Device Establishment).'' Dated: April 29, 2004. Jeffrey Shuren, Assistant Commissioner for Policy. [FR Doc. 04-10265 Filed 5-6-04; 8:45 am] BILLING CODE 4160-01-S