BAXTER DUPLOTIP SURGICAL SEALANT APPLICATOR

BAXTER DUPLOTIP SURGICAL SEALANT APPLICATOR is an FDA 510(k)-cleared medical device (K033589) manufactured by Micromedics, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 3, 2004. Regulation: 8.