This webinar will discuss the new draft guidance document from the FDA: "510(k) Device Modifications: Deciding When to Submit a 510(k) for a Change to an Existing Device", dated July 27, 2011.
FDA's Revised [Draft] Guidance on Medical Device Changes and the 510(k) - Webinar By GlobalCompliancePanel
25 January 2012, Wilmington, United States
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Online Training, 1000 N West Street,, Delaware, Suite 1200, Wilmington, 19801, United States
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