SOMNUS MODEL S2 ELECTROSURGICAL GENERATOR

SOMNUS MODEL S2 ELECTROSURGICAL GENERATOR is an FDA 510(k)-cleared medical device (K001438) manufactured by Somnus Medical Technologies, 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 May 15, 2000. Regulation: 8.