'Medical device manufacturers understand' presentation slideshows

510(K) Submission - A Comprehensive and an Updated Overview

Why should you attend: The section [510(k)] of the Federal Food, Drug, and Cosmetic Act (FD&C Act or the Act) prescribes the premarket notification requirements. The premarket notification [510(k)] is the most common pathway to market for medical devices including in vitro diagnostic medical devices (IVDs). For More Details: Email: david@grcts.com Tel: 1-248-233-2049 Web: www.grcts.com

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