
Beckman Coulter, Inc.
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UNICEL DXH 800 COULTER CELLULAR ANALYSIS SYSTEM is an FDA 510(k)-cleared medical device (K081930) manufactured by Beckman Coulter, Inc.. This device is classified under the Hematology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 18, 2008. Regulation: 8.