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Errors Corrected in Device Reporting Rule

05/07/2004
Federal Register Final rule: FDA is correcting inadvertent errors in a 4/8 Federal Register final rule that corrected a 3/10 FR final rule on Medical Device Reports; reports of corrections and removals; establishment registration and device listing: premarket approval supplements; quality system regulation; and importation of electronic products. To view this final rule, click here.

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