Laser Optik Systeme GmbH & Co. KG

Laser Optik Systeme GmbH & Co. KG — FDA 510(k) Submissions

Laser Optik Systeme GmbH & Co. KG has submitted 7 FDA 510(k) premarket notifications since 1994, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, General & Plastic Surgery, Light Source, Endoscope, Xenon Arc, Endoscope, Rigid, Source, Carrier, Fiberoptic Light . Use the specialty filter in the sidebar to narrow results.