
Beckman Coulter, Inc.
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DxC 700 AU Clinical Chemistry Analyzer, AU IgG Reagent is an FDA 510(k)-cleared medical device (K162208) manufactured by Beckman Coulter, Inc.. This device is classified under the Immunology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 8, 2017. Regulation: 8.