Imactis, Sas is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Imactis, Sas - FDA 510(k) Cleared Devices
Recent clearances: IMACTIS CT-Navigation system
1
Total
1
Cleared
0
Denied
Imactis, Sas has 1 FDA 510(k) cleared medical devices. Based in La Tronche, FR.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Imactis, Sas Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Imactis, Sas
1 devices