KARL STORZ INSTRUMENTS FOR BIPOLAR COAGULATION

KARL STORZ INSTRUMENTS FOR BIPOLAR COAGULATION is an FDA 510(k)-cleared medical device (K936036) manufactured by KARL STORZ Endoscopy-America, Inc.. 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 June 19, 1994. Regulation: 8.