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FDA > CDRH > Reprocessing of Single-Use Devices > MDUFMA

Medical Device User Fee and Modernization Act (MDUFMA) of 2002 - "FAQ's" Pertaining to Reprocessed Single-Use Devices

On October 26, 2002, President Bush signed into law the Medical Device User Fee and Modernization Act of 2002 (MDUFMA), P.L. 107-250, amending the Federal Food, Drug, and Cosmetic Act ( the Act). The following frequently-asked-questions (FAQs) pertain to the provisions regarding reprocessed single-use devices.

Background Information Questions and Answers

Reprocessed Single-Use Devices Questions and Answers

Updated November 25, 2002

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