Urogen Pharma, Ltd.

Urogen Pharma, Ltd. — FDA 510(k) Submissions

Urogen Pharma, Ltd. has submitted 5 FDA 510(k) premarket notifications since 2018, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Piston Syringe Lever, Catheter, Urological . Use the specialty filter in the sidebar to narrow results.