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Medlogic Global , Ltd.
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LIQUIBAND ULTIMA, MODEL LB0004 is an FDA 510(k)-cleared medical device (K083531) manufactured by Medlogic Global , Ltd.. 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 February 11, 2009. Regulation: 8.