CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURG

CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURG is an FDA 510(k)-cleared medical device (K914883) manufactured by Circon Video. 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 January 14, 1993. Regulation: 8.