Rz Medizintechnik GmbH

Rz Medizintechnik GmbH — FDA 510(k) Submissions

Rz Medizintechnik GmbH has submitted 3 FDA 510(k) premarket notifications since 2008, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrosurgical, Cutting & Coagulation & Accessories, Arthroscope, Hysteroscope (and Accessories) . Use the specialty filter in the sidebar to narrow results.