Keyword Analysis & Research: 510k versus pma


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Who is required by the FDA to file a 510k?

Each person who wants to market in the U.S., a Class I, II, and III device intended for human use, for which a Premarket Approval application (PMA) is not required, must submit a 510 (k) to FDA...

What is 510K clearance?

510(k) Clearance. The purpose of a 510(k) submission is to demonstrate that a device is “substantially equivalent” to a predicate device (one that has been cleared by the FDA or marketed before 1976).


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