AUTOCON II 200 ELECTROSURGICAL GENERATOR

AUTOCON II 200 ELECTROSURGICAL GENERATOR is an FDA 510(k)-cleared medical device (K023924) manufactured by Karl Storz Endoscopy. 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 20, 2003. Regulation: 8.