Intrasense is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Intrasense - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
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