Medical Device Manufacturer · US , Bridgeport , WV

Pertrach - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1989

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Pertrach Anesthesiology ✕

2 devices

1-2 of 2

Cleared Jul 10, 1992

EMERGENCY PERCUTANEOUS CRICOTHYROIDOTOMY KIT,MODIF

Anesthesiology · 273d

Cleared May 25, 1989

MODIFIED ADULT CRICOTHYROIDOTOMY KIT

Anesthesiology · 161d