Fujifilm Corporaton

Fujifilm Corporaton — FDA 510(k) Submissions

Fujifilm Corporaton has submitted 6 FDA 510(k) premarket notifications since 2020, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, General & Plastic Surgery, System, Image Processing, Radiological, Bronchoscope (flexible Or Rigid), Gastroscope And Accessories, Flexible/rigid, Enteroscope And Accessories . Use the specialty filter in the sidebar to narrow results.