Randwal Instrument Co., Inc.

Randwal Instrument Co., Inc. — FDA 510(k) Submissions

Randwal Instrument Co., Inc. has submitted 6 FDA 510(k) premarket notifications since 1983, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ophthalmoscope, Battery-powered, Instrument, Visual Field, Laser, Photostimulator, Ac-powered . Use the specialty filter in the sidebar to narrow results.