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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...

When is a 510k required?

A premarket notification (510(k)) is required when a legally marketed device subject to 510(k) requirements is significantly changed or modified in design, components, method of manufacture, or intended use.

What does FDA 510 k cleared mean?

FDA clearance through the 510 (k) process means the agency is in agreement with the manufacturer that a medical device is similar to a previously approved product. In making that determination, the FDA will conclude a device is substantially equivalent to a marketed device if:


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