Ya-Man, Ltd.

Ya-Man, Ltd. — FDA 510(k) Submissions

Ya-Man, Ltd. has submitted 6 FDA 510(k) premarket notifications since 2001, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Transcutaneous Electrical, Aesthetic Purposes, Powered Laser Surgical Instrument, Lamp, Infrared, Therapeutic Heating . Use the specialty filter in the sidebar to narrow results.