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What is a 510 k medical device?

A 510 (k) is a premarket submission made to FDA to demonstrate that the device to be marketed is at least as safe and effective, that is, substantially equivalent, to a legally marketed device (21 CFR 807.92 (a) (3)) that is not subject to PMA.

What is a 510k number?

A 510(K) is a premarket submission made to FDA to demonstrate that the device to be marketed is at least as safe and effective, that is, substantially equivalent, to a legally marketed device (21 CFR §807.92(a)(3)) that is not subject to premarket approval. Learn more...

What is 510k FDA approval?

FDA 510(k) is a premarket submission made to FDA to demonstrate that the device to be marketed is at least as safe and effective, that is, substantially equivalent, to a legally marketed device that is not subject to premarket approval (PMA).

What is 510 k exempt?

The FDA website provides some great information. 510 (k) exempt medical devices: Medical devices that do not require FDA review before the devices are marketed are considered “510 (k) exempt.” These medical devices are mostly low-risk, Class I devices and some Class II devices...


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