Siemens Healthcare Diagnostic Products GmbH

Siemens Healthcare Diagnostic Products GmbH — FDA 510(k) Submissions

Siemens Healthcare Diagnostic Products GmbH has submitted 4 FDA 510(k) premarket notifications since 2016, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Multipurpose For In Vitro Coagulation Studies, System, Test, C-reactive Protein, Antithrombin Iii Quantitation . Use the specialty filter in the sidebar to narrow results.