Anhui Tiankang Medical Technology Co., Ltd.

Anhui Tiankang Medical Technology Co., Ltd. — FDA 510(k) Submissions

Anhui Tiankang Medical Technology Co., Ltd. has submitted 12 FDA 510(k) premarket notifications since 2019, of which 12 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Syringe, Piston, Needle, Hypodermic, Single Lumen, Syringe, Antistick, Set, Administration, Intravascular, Mask, Surgical . Use the specialty filter in the sidebar to narrow results.