Reichert, Inc.

Reichert, Inc. — FDA 510(k) Submissions

Reichert, Inc. has submitted 9 FDA 510(k) premarket notifications since 2004, of which 9 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Biomicroscope, Slit-lamp, Ac-powered, Tonometer, Ac-powered, Tonometer, Manual, System, Imaging, Pulsed Echo, Ultrasonic, Tomography, Optical Coherence . Use the specialty filter in the sidebar to narrow results.