Chattanooga Group, Inc.

Chattanooga Group, Inc. — FDA 510(k) Submissions

Chattanooga Group, Inc. has submitted 70 FDA 510(k) premarket notifications since 1980, of which 68 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Muscle, Powered, Stimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat, Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat, Stimulator, Nerve, Transcutaneous, For Pain Relief, Dynamometer, Ac-powered . Use the specialty filter in the sidebar to narrow results.