[Federal Register: May 7, 2004 (Volume 69, Number 89)]
[Rules and Regulations]
[Page 25489]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr07my04-6]
[[Page 25489]]
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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.
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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