Medical Device Manufacturer · US , Bonita Springs , FL

Activaero America, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2007

Total

Cleared

Denied

Activaero America, Inc. has 3 FDA 510(k) cleared medical devices. Based in Bonita Springs, US.

Historical record: 3 cleared submissions from 2007 to 2009. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Activaero America, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Activaero America, Inc.

3 devices

1-3 of 3