
Cytomedix
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AUTOLOGEL PROCESS CENTRIFUGE, MODEL B4360 (100-103, 100-129) is an FDA 510(k)-cleared medical device (K030340) manufactured by Cytomedix. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on April 10, 2003. Regulation: 8.