FDA Presentation: 510(k) Format Guidance, Including Standards Form, and Extensions/Clinical Trial Form and 510(k)

(This presentation is also available in video format with captioning and PDF printer-friendly format.)

Marjorie Shulman
Office of Device Evaluation
Program Operations Staff
Premarket Notification Staff

Marjorie.Shulman@fda.hhs.gov
(240) 276-4040

27 slides Updated November 19, 2008

/uploads/soft/200812/1_22212528.rar

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