AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240

AARON 1200 HIGH FREQUENCY ELECTROSURGICL GENERATOR A1200, A1200/240 is an FDA 510(k)-cleared medical device (K980366) 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 February 26, 1998. Regulation: 8.