Conmedcorp
Conmedcorp — FDA 510(k) Submissions
Conmedcorp has submitted 92 FDA 510(k) premarket notifications since 1981, of which 92 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Electrosurgical, Cutting & Coagulation & Accessories, Laparoscope, General & Plastic Surgery, Electrode, Electrocardiograph, Electrode, Cutaneous, Laparoscope, Gynecologic (and Accessories) . Use the specialty filter in the sidebar to narrow results.
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