Diagnostica Stago S.A.S

Diagnostica Stago S.A.S — FDA 510(k) Submissions

Diagnostica Stago S.A.S has submitted 3 FDA 510(k) premarket notifications since 2015, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Multipurpose For In Vitro Coagulation Studies, Test, Time, Prothrombin . Use the specialty filter in the sidebar to narrow results.