AARON 2100 HIGH FREQUENCY ELECTROSURGICAL GENERATOR

AARON 2100 HIGH FREQUENCY ELECTROSURGICAL GENERATOR is an FDA 510(k)-cleared medical device (K001382) manufactured by Aaron Medical Industries. 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 26, 2000. Regulation: 8.