National Advanced Endoscopy Devices, Inc.

National Advanced Endoscopy Devices, Inc. — FDA 510(k) Submissions

National Advanced Endoscopy Devices, Inc. has submitted 8 FDA 510(k) premarket notifications since 1999, of which 8 received clearance as substantially equivalent to a predicate device.

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