Parker Laboratories, Inc.

Parker Laboratories, Inc. — FDA 510(k) Submissions

Parker Laboratories, Inc. has submitted 30 FDA 510(k) premarket notifications since 1977, of which 30 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Media, Electroconductive, System, Imaging, Pulsed Echo, Ultrasonic, Resin, Denture, Relining, Repairing, Rebasing, Transducer, Ultrasonic, Diagnostic, Cement, Dental . Use the specialty filter in the sidebar to narrow results.