Medical Device Manufacturer · US , Tuscaloosa , AL

Cwt Workshop - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1990

Total

Cleared

Denied

Cwt Workshop has 1 FDA 510(k) cleared medical devices. Based in Tuscaloosa, US.

Historical record: 1 cleared submissions from 1990 to 1990. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Cwt Workshop Filter by specialty or product code using the sidebar.

Cwt Workshop 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 - Cwt Workshop

1 devices

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