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510(k) Submissions: Requirements, Challenges and Successful Clearance - Webinar By GlobalCompliancePanel

19 April 2012, Wilmington, United States


Introduction
A premarket notification [510(k)] submission is the most common pathway to market for medical devices including in vitro diagnostic devices.

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Venue
OnlineTraining

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

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Organised by
GlobalCompliancePanel
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