DESERET CAPACITY PLUS ELECTROSURG. PAD

DESERET CAPACITY PLUS ELECTROSURG. PAD is an FDA 510(k)-cleared medical device (K821356) manufactured by Warner-Lambert 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 July 13, 1982. Regulation: 8.