Jiangxi Sanxin Medtec Co., Ltd.

Jiangxi Sanxin Medtec Co., Ltd. — FDA 510(k) Submissions

Jiangxi Sanxin Medtec Co., Ltd. has submitted 3 FDA 510(k) premarket notifications since 2015, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days, Mask, Surgical, Set, Tubing, Blood, With And Without Anti-regurgitation Valve . Use the specialty filter in the sidebar to narrow results.