Wells Johnson Co.

Wells Johnson Co. — FDA 510(k) Submissions

Wells Johnson Co. has submitted 15 FDA 510(k) premarket notifications since 1983, of which 15 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cannula, Surgical, General & Plastic Surgery, Instrument, Ultrasonic Surgical, Stocking, Medical Support (to Prevent Pooling Of Blood In Legs), Expander, Surgical, Skin Graft, Pump, Portable, Aspiration (manual Or Powered) . Use the specialty filter in the sidebar to narrow results.