Ito Co., Ltd.

Ito Co., Ltd. — FDA 510(k) Submissions

Ito Co., Ltd. has submitted 8 FDA 510(k) premarket notifications since 1999, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat, Equipment, Traction, Powered, Stimulator, Muscle, Powered, Dental, Stimulator, Muscle, Powered, Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat . Use the specialty filter in the sidebar to narrow results.