AARON 1250 HIGH FREQUENCY ELECTROSURGICAL GENERATOR, MODEL A1250

AARON 1250 HIGH FREQUENCY ELECTROSURGICAL GENERATOR, MODEL A1250 is an FDA 510(k)-cleared medical device (K001955) 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 December 21, 2000. Regulation: 8.