GYRUS PLASMACISION AND PLASMABLEND ELECTRODES

GYRUS PLASMACISION AND PLASMABLEND ELECTRODES is an FDA 510(k)-cleared medical device (K050460) manufactured by Gyrus Medical, 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 October 24, 2005. Regulation: 8.