Rules and Regulations. Final rule; technical amendment; correction

268 words·~1 min read·/register/2004/05/07/04-10265

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BILLING CODE 4910-13-P 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.” § 807.22 [Corrected] 2. On page 18473, in the first column, in § 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]

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Rules and Regulations

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