REPROCESSED SURGICAL ELECTRIC INSTRUMENT

REPROCESSED SURGICAL ELECTRIC INSTRUMENT is an FDA 510(k)-cleared medical device (K120040) manufactured by Sterilmed, 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 October 4, 2012. Regulation: 8.