Conphar, Inc.

Conphar, Inc. — FDA 510(k) Submissions

Conphar, Inc. has submitted 122 FDA 510(k) premarket notifications since 1979, of which 122 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cutter, Surgical, Forceps, General & Plastic Surgery, Blood Pressure Cuff, Collector, Urine, (and Accessories) For Indwelling Catheter, Scissors, Surgical Tissue, Dental . Use the specialty filter in the sidebar to narrow results.