Changsha Anxiang Medical Technology Co., Ltd.

Changsha Anxiang Medical Technology Co., Ltd. — FDA 510(k) Submissions

Changsha Anxiang Medical Technology Co., Ltd. has submitted 8 FDA 510(k) premarket notifications since 2024, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stimulator, Muscle, Powered, For Muscle Conditioning, Stimulator, Nerve, Transcutaneous, Over-the-counter . Use the specialty filter in the sidebar to narrow results.