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.

Athena Gtx 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 - Athena Gtx

7 devices

1-7 of 7