Medical Device Manufacturer · US , Dana Point , CA

Ekom S.R.O. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2006

Total

Cleared

Denied

Ekom S.R.O. has 2 FDA 510(k) cleared medical devices. Based in Dana Point, US.

Historical record: 2 cleared submissions from 2006 to 2009. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Ekom S.R.O. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ekom S.R.O.

2 devices

1-2 of 2