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Title: Webinar Medical Device Changes and the 510(k) - PowerPoint PPT Presentation
Description: This webinar will provide valuable guidance to regulated companies in development and implementation of formal, defined, documented methods for analysis of product changes and when to file a new 510(k). Consideration of the U.S. FDA's current K-97-1 Memo / guidance document on "510(k) Device Modifications" – PowerPoint PPT presentation
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