REPROCESSED LIGASURE BLUNT TIP LAPAROSCOPIC SEALER/DIVIDER

REPROCESSED LIGASURE BLUNT TIP LAPAROSCOPIC SEALER/DIVIDER is an FDA 510(k)-cleared medical device (K133578) manufactured by Stryker Sustainability 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 April 9, 2014. Regulation: 8.