Brosmed Medical Co., Ltd.

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

Brosmed Medical Co., Ltd. has submitted 8 FDA 510(k) premarket notifications since 2016, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Angioplasty, Peripheral, Transluminal, Catheters, Transluminal Coronary Angioplasty, Percutaneous, Catheter, Percutaneous, Cutting/scoring . Use the specialty filter in the sidebar to narrow results.