Navigating 510k and De Novo Requirements
August
02

Navigating 510k and De Novo Requirements

 August 2 to August 5, 2021 

It is an online event.


This 4-day course will navigate the 510(K) clearance process and De Novo classifications requests for the United States (U.S.) and Global Medical Device Manufacturers and regulatory affairs leaders to improve the ability to bring new and improved devices to the U.S. marketplace.

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