Medical Device Manufacturer · US , Bellaire , TX

Prucka Engineering, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1989

Total

Cleared

Denied

Prucka Engineering, Inc. has 6 FDA 510(k) cleared medical devices. Based in Bellaire, US.

Historical record: 6 cleared submissions from 1989 to 2000. Primary specialty: Cardiovascular.

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

Prucka Engineering, 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 - Prucka Engineering, Inc.

6 devices

1-6 of 6