Medical Device Manufacturer · US , Newport Beach , CA

Promedica Products, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1988

Total

Cleared

Denied

Promedica Products, Inc. has 6 FDA 510(k) cleared medical devices. Based in Newport Beach, US.

Historical record: 6 cleared submissions from 1988 to 1992. Primary specialty: General Hospital.

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

Promedica Products, 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 - Promedica Products, Inc.

6 devices

1-6 of 6