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Introduction

This webinar is intended to demonstrate how to prepare a 510(k) in an adequate manner with increased quality to expedite the streamlined review process. The premarket notification [510(k)] is the most common pathway to market for medical devices including in vitro diagnostic medical devices.

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Venue

Online Training

Livermore Common, Online Training, California, Fremont, 94539, United States

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Organised by

GlobalCompliancePanel

Contact information

Mr John Robinson
Livermore Common | Fremont | CA | 94539, Fremont, 94539, United States of America
8004479407
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