Terumo Medical Products Hangzhou Co., Ltd.

Terumo Medical Products Hangzhou Co., Ltd. — FDA 510(k) Submissions

Terumo Medical Products Hangzhou Co., Ltd. has submitted 5 FDA 510(k) premarket notifications since 2003, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Set, Administration, Intravascular, Guide, Wire, Catheter, Neurovasculature, Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days, Midline Catheter . Use the specialty filter in the sidebar to narrow results.