SOMNUS TISSUE COAGULATING ELECTRODE

SOMNUS TISSUE COAGULATING ELECTRODE is an FDA 510(k)-cleared medical device (K973701) 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 January 29, 1998. Regulation: 8.