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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 does 510K clearance 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:

When do you need a 510k?

If you are planning to manufacture or distribute a medical device within the United States of America, the FDA requires (in most cases) that you complete either a 510k submission or obtain premarket approval for your medical device.

What is 510 k process?

FDA’s 510(k) pre-market review process for medical devices provides strong protections to American patients and promotes medical innovation. It provides FDA the flexibility it needs to ensure the safety and effectiveness of low- and moderate-risk medical devices whose risks are well-understood from experience with similar devices.


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