Medical Device Manufacturer · US , Independence , MO

Action Labs, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1993

Total

Cleared

Denied

Action Labs, Inc. has 1 FDA 510(k) cleared medical devices. Based in Independence, US.

Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Action Labs, Inc. Filter by specialty or product code using the sidebar.

Action Labs, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Action Labs, Inc.

1 devices

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