Medical Device Manufacturer · US , Carmel , IN

Ameriflo Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2004

Total

Cleared

Denied

Ameriflo Corp. has 2 FDA 510(k) cleared medical devices. Based in Carmel, US.

Historical record: 2 cleared submissions from 2004 to 2006. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Ameriflo Corp.

2 devices

1-2 of 2