Percutaneous Systems, Inc.

Percutaneous Systems, Inc. — FDA 510(k) Submissions

Percutaneous Systems, Inc. has submitted 6 FDA 510(k) premarket notifications since 2004, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Accessories, Catheter, G-u, Dislodger, Stone, Basket, Ureteral, Metal, Catheter, Straight . Use the specialty filter in the sidebar to narrow results.