REPROCESSED LIGASURE VESSEL SEALER/DIVIDER

REPROCESSED LIGASURE VESSEL SEALER/DIVIDER is an FDA 510(k)-cleared medical device (K062525) manufactured by Ascent Healthcare Solutions. 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, 2007. Regulation: 8.