Zmi Electronics , Ltd.

Zmi Electronics , Ltd. — FDA 510(k) Submissions

Zmi Electronics , Ltd. has submitted 3 FDA 510(k) premarket notifications since 2018, of which 3 received clearance as substantially equivalent to a predicate device.

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