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.

Airon Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Airon Corporation

4 devices

1-4 of 4