
Implant Innovations, Inc.
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3I MODEL(S)7426 AND 7427 CELSEP CENTRIFUGE SYSTEM is an FDA 510(k)-cleared medical device (K994148) manufactured by Implant Innovations, Inc.. This device is classified under the Clinical Chemistry specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on January 31, 2000. Regulation: 8.