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Business · 10/01/2003

FDA Corrects Notice on Medical Device User Fees for Fiscal Year 2003

The Food and Drug Administration (FDA) is correcting a notice that appeared in the Federal Register on November 21, 2002, to clarify the fee for small businesses submitting 510(k) premarket notifications for FDA review during fiscal year 2003.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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