LIGASURE VESSEL SEALING SYSTEM. LIGASURE INSTRUMENTS

LIGASURE VESSEL SEALING SYSTEM. LIGASURE INSTRUMENTS is an FDA 510(k)-cleared medical device (K043273) manufactured by Valleylab. 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 4, 2005. Regulation: 8.