Superior Healthcare Group, Inc.

Superior Healthcare Group, Inc. — FDA 510(k) Submissions

Superior Healthcare Group, Inc. has submitted 14 FDA 510(k) premarket notifications since 1985, of which 13 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tubes, Gastrointestinal (and Accessories), Latex Patient Examination Glove, Endoscopic Irrigation/suction System, Catheters, Suction, Tracheobronchial, Tray, Catheterization, Sterile Urethral, With Or Without Catheter (kit) . Use the specialty filter in the sidebar to narrow results.