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

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.

Regulatory submissions have been managed by Regulatory Technology Services, LLC and Navigant Consulting, Inc..