MODEL FORCE 2 ELECTROSURGICAL GENERATOR

MODEL FORCE 2 ELECTROSURGICAL GENERATOR is an FDA 510(k)-cleared medical device (K844403) manufactured by Valleylab, 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 February 19, 1985. Regulation: 8.