Medical Device Manufacturer · US , Wyckoff , NJ

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

5 submissions · 5 cleared · Since 1994

Total

Cleared

Denied

Promedical , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Wyckoff, US.

Historical record: 5 cleared submissions from 1994 to 1995. Primary specialty: Gastroenterology & Urology.

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

Promedical , 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 - Promedical , Ltd.

5 devices

1-5 of 5