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Thermogenesis Corp.
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AXP PLATFORM MARROW XPRESS SYSTEM MODEL 8-5137, 8-5138, 8-5139, 8-5140 (PRIMARY) is an FDA 510(k)-cleared medical device (K081345) manufactured by Thermogenesis Corp.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 9, 2008. Regulation: 8.