Dragerwerk AG & CO Kgaa

Dragerwerk AG & CO Kgaa — FDA 510(k) Submissions

Dragerwerk AG & CO Kgaa has submitted 2 FDA 510(k) premarket notifications since 2019, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ventilator, Continuous, Facility Use, Incubator, Neonatal . Use the specialty filter in the sidebar to narrow results.