
Covidien, Formerly Valleylab, A Division of Tyco H
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LIGASURE 5 MM MARYLAND JAW SEALER/DIVIDER ONE-STEP SEALING (LF 17XX) is an FDA 510(k)-cleared medical device (K133338) manufactured by Covidien, Formerly Valleylab, A Division of Tyco H. 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 December 19, 2013. Regulation: 8.