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Device Changes and the 510(k) - Webinar By GlobalCompliancePanel

9 May 2012, Wilmington, United States


Introduction
The majority of medical devices are cleared for marketing in the U.S. by the FDA under the 510(k) process.

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Venue
Online Training

Online Training, 1000 N West Street, Delaware, Suite 1200, Wilmington, 19801, United States

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Organised by
GlobalCompliancePanel
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