Gimmi GmbH

Gimmi GmbH — FDA 510(k) Submissions

Gimmi GmbH has submitted 6 FDA 510(k) premarket notifications since 2001, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Hysteroscope (and Accessories), Endoscopic Video Imaging System/component, Gastroenterology-urology, Bronchoscope (flexible Or Rigid), Clip, Aneurysm, Light Source, Endoscope, Xenon Arc . Use the specialty filter in the sidebar to narrow results.