Welcon, Inc.

Welcon, Inc. — FDA 510(k) Submissions

Welcon, Inc. has submitted 8 FDA 510(k) premarket notifications since 1981, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter And Tip, Suction, Syringe, Irrigating (non Dental), Catheter, Urological, Light, Surgical, Accessories, Tray, Catheterization, Sterile Urethral, With Or Without Catheter (kit) . Use the specialty filter in the sidebar to narrow results.