Dr?gerwerk AG & Co KGaA

Dr?gerwerk AG & Co KGaA — FDA 510(k) Submissions

Dr?gerwerk AG & Co KGaA has submitted 4 FDA 510(k) premarket notifications since 2022, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Filter, Bacterial, Breathing-circuit, Gas-machine, Anesthesia, Incubator, Neonatal, Cable, Transducer And Electrode, Patient, (including Connector) . Use the specialty filter in the sidebar to narrow results.