Medical Device Manufacturer · FR , Toulose

Intrasense - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2007

Total

Cleared

Denied

Intrasense has 3 FDA 510(k) cleared medical devices. Based in Toulose, FR.

Historical record: 3 cleared submissions from 2007 to 2012. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Intrasense

3 devices

1-3 of 3