Microcurrent Research, Inc.

Microcurrent Research, Inc. — FDA 510(k) Submissions

Microcurrent Research, Inc. has submitted 4 FDA 510(k) premarket notifications since 1989, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Muscle, Powered, Dental, Stimulator, Nerve, Transcutaneous, For Pain Relief . Use the specialty filter in the sidebar to narrow results.