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Beckman Coulter Diagnostics, a leader in clinical diagnostics, has announced that its new DxC 500i Clinical Analyzer has received 510(k) clearance from the U.S. Food and Drug Administration. This integrated analyzer combines advanced technology with an intuitive user interface, designed to help laboratories of all sizes manage increasing healthcare demands. The DxC 500i offers a throughput of up to 800 clinical chemistry tests per hour and 100 immunoassay tests per hour, providing precise and reliable results essential for timely clinical decision-making. The company also highlights recent advancements, including a new assay earning CE Mark for bacterial vs. viral infection results in approximately 20 minutes, and a fully automated BD-Tau research immunoassay test to advance neurodegenerative clinical research.