Medical Device Manufacturer · US , Alpharetta , GA

Koo Americas, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2005

Recent clearances: KOO AMERICAS VALVE PEEP, MODEL KM-809

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Koo Americas, Inc. Anesthesiology ✕

1 devices

1-1 of 1

Cleared Jun 06, 2005

KOO AMERICAS VALVE PEEP, MODEL KM-809

Anesthesiology · 55d