BOVIE CONDUCTIVE ADHES-DISPER-ELECTRO

BOVIE CONDUCTIVE ADHES-DISPER-ELECTRO is an FDA 510(k)-cleared medical device (K834048) manufactured by Castle 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 April 3, 1984. Regulation: 8.