Hantech Medical Device Co., Ltd.

Hantech Medical Device Co., Ltd. — FDA 510(k) Submissions

Hantech Medical Device Co., Ltd. has submitted 5 FDA 510(k) premarket notifications since 2022, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Needle, Hypodermic, Single Lumen, Mask, Surgical, Syringe, Piston, Saline, Vascular Access Flush . Use the specialty filter in the sidebar to narrow results.