Wuxi Jiajian Medical Instrument Co., Ltd.

Wuxi Jiajian Medical Instrument Co., Ltd. — FDA 510(k) Submissions

Wuxi Jiajian Medical Instrument Co., Ltd. has submitted 12 FDA 510(k) premarket notifications since 2009, of which 12 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Nerve, Transcutaneous, For Pain Relief, Stimulator, Electro-acupuncture, Electrode, Cutaneous, Stimulator, Nerve, Transcutaneous, Over-the-counter, Needle, Acupuncture, Single Use . Use the specialty filter in the sidebar to narrow results.