Medical Device Manufacturer · FR , Aix En Provence

Dyn'R Sas - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2012

Total

Cleared

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

1-1 of 1