FDA's 2011 Revised 510(k) Premarket Notification Process

8 April 2011, Palo Alto, United States


Introduction
This 510(K) training will help you understand and be prepared for substantial changes to the Premarket Notification 510(k) process for Class II medical devices.
Venue
Online Event

Online Event, 2600 E. Bayshore Road, Palo Alto, 94303, United States

Organised by
ComplianceOnline
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