Dyn'R Sas is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Dyn'R Sas - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Dyn'R Sas has 1 FDA 510(k) cleared medical devices. Based in Aix En Provence, FR.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Dyn'R Sas Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dyn'R Sas
1 devices