Medical Device Manufacturer · US , Mchenry , IL

Surgitek - FDA 510(k) Cleared Devices

29 submissions · 28 cleared · Since 1983

29

Total

28

Cleared

0

Denied

FDA 510(k) Regulatory Record - Surgitek Anesthesiology ✕

1 devices

1-1 of 1

Cleared Dec 27, 1983

BRONCHOSCOPY TUBE W/ULTRA LOCUFF

Anesthesiology · 95d