Medical Device Regulations: Premarket Notification-The 510(K) Process Movie Review 1984

Information and Film Reviews for Medical Device Regulations: Premarket Notification-The 510(K) Process the Movie

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This video describes the Food & Drug Administration's process for screening medical devices before they can be put on the market.

Distribution

National Audiovisual Center, 5285 Port Royal Rd., Springfield, VA 22161, Phone: (703)605-4603, Toll-free: 800-553-6847, Fax: (703)321-8547, Email: orders@ntis.fedworld.gov, URL: http://www.ntis.gov/products/nac/index.asp

Available on VHS
Running time 35 minutes.

Cast and Crew

Genres
Medical Care
Producer
USCRDH

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