B. Braun Melsugen AG

B. Braun Melsugen AG — FDA 510(k) Submissions

B. Braun Melsugen AG has submitted 1 FDA 510(k) premarket notifications since 2020, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Accessories, Pump, Infusion . Use the specialty filter in the sidebar to narrow results.