Easymed Instruments Co., Ltd.

Easymed Instruments Co., Ltd. — FDA 510(k) Submissions

Easymed Instruments Co., Ltd. has submitted 3 FDA 510(k) premarket notifications since 2014, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Nerve, Transcutaneous, Over-the-counter, Stimulator, Electrical, Non-implantable, For Incontinence . Use the specialty filter in the sidebar to narrow results.