Medical Device Manufacturer · US , Carmel , IN

Ameriflo Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2004

Recent clearances: FLO-RITE, MODEL 478-1, FLO-RITE

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Ameriflo Corp. Anesthesiology ✕

2 devices

1-2 of 2

Cleared Apr 19, 2006

FLO-RITE, MODEL 478-1

Anesthesiology · 64d

Cleared Aug 12, 2004

Anesthesiology · 111d