Medical Device Manufacturer · US , Bridgeport , WV

Pertrach - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1989

Total

Cleared

Denied

Pertrach has 2 FDA 510(k) cleared medical devices. Based in Bridgeport, US.

Historical record: 2 cleared submissions from 1989 to 1992. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Pertrach

2 devices

1-2 of 2