
LeMaitre Vascular, Inc.
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ANASTOCLIP MODELS 4001-01, 4000-02, 4000-03, 4000-04, 4004-01, 4004-02, ANASTOCLIP is an FDA 510(k)-cleared medical device (K091987) manufactured by LeMaitre Vascular, Inc.. 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 22, 2010. Regulation: 8.