Van-Tec, Inc.

Van-Tec, Inc. — FDA 510(k) Submissions

Van-Tec, Inc. has submitted 52 FDA 510(k) premarket notifications since 1982, of which 52 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Dislodger, Stone, Basket, Ureteral, Metal, Catheter, Urological, Instrument, Biopsy, Dilator, Catheter, Ureteral, Stent, Ureteral . Use the specialty filter in the sidebar to narrow results.