Medical Device Manufacturer · US , Melbourne , FL

Airon Corporation - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2003

Total

Cleared

Denied

Airon Corporation has 4 FDA 510(k) cleared medical devices. Based in Melbourne, US.

Historical record: 4 cleared submissions from 2003 to 2012. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Airon Corporation

4 devices

1-4 of 4