
Fisher Scientific Co., LLC
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MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGE is an FDA 510(k)-cleared medical device (K915441) manufactured by Fisher Scientific Co., LLC. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 7, 1992. Regulation: 8.