Medical Device Manufacturer · US , Des Moines , IA

Athena Gtx - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2010

Total

Cleared

Denied

Athena Gtx has 7 FDA 510(k) cleared medical devices. Based in Des Moines, US.

Historical record: 7 cleared submissions from 2010 to 2020. Primary specialty: Cardiovascular.

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

FDA 510(k) cleared devices by Athena Gtx

7 devices

1-7 of 7