Sunlamp products & UV Lamps: 3 months to submit 510(k)s to FDA

Registrar Corp's U.S. FDA News blog provides regulatory updates for FDA regulated industries. Registrar Corp helps medical device establishments comply with FDA regulations, such as registration, listing, UDI and GUDID requirements, 510(k) requirements, and more.

By David Lennarz, Vice President and Co-Founder of Registrar Corp

Food & Drug Administration (FDA)

News Well, Blog, Food & Drug Administration (FDA), Regulatory/Compliance

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