STORZ S2050 SERIES BIPOLAR FORCEPS

STORZ S2050 SERIES BIPOLAR FORCEPS is an FDA 510(k)-cleared medical device (K960009) manufactured by Storz Instrument Co.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 5, 1996. Regulation: 8.