
Bd Becton Dickinson Vacutainer Systems Preanalytic
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FIBROSYSTEM is an FDA 510(k)-cleared medical device (K823520) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Hematology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on December 27, 1982. Regulation: 8.