
Somnus Medical Technologies, Inc.
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ELECTROSURGICAL GENERATOR, MODEL S1 is an FDA 510(k)-cleared medical device (K000501) 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 March 16, 2000. Regulation: 8.