Uresil Corp.

Uresil Corp. — FDA 510(k) Submissions

Uresil Corp. has submitted 45 FDA 510(k) premarket notifications since 1981, of which 44 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stents, Drains And Dilators For The Biliary Ducts, Catheter, Nephrostomy, Catheter, Percutaneous, Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass, Catheter, Ventricular, General & Plastic Surgery . Use the specialty filter in the sidebar to narrow results.