Medical Device Manufacturer · US , State College , PA

Proact, Ltd. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1990

Total

Cleared

Denied

Proact, Ltd. has 5 FDA 510(k) cleared medical devices. Based in State College, US.

Historical record: 5 cleared submissions from 1990 to 1994. Primary specialty: Gastroenterology & Urology.

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

Proact, Ltd. 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 - Proact, Ltd.

5 devices

1-5 of 5