Medical Device Manufacturer · US , Carmel , IN

Esaote Europe B.V. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2006

Total

Cleared

Denied

Esaote Europe B.V. has 7 FDA 510(k) cleared medical devices. Based in Carmel, US.

Historical record: 7 cleared submissions from 2006 to 2016. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Esaote Europe B.V. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Esaote Europe B.V.

7 devices

1-7 of 7