ACUCISE ELECTROSURGICAL TROCAR

ACUCISE ELECTROSURGICAL TROCAR is an FDA 510(k)-cleared medical device (K925984) manufactured by Applied Medical Resources. 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 16, 1993. Regulation: 8.