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NEW YORK – Beckman Coulter's DxA 5000 total laboratory automation solution received FDA 510(k) clearance and is now available for sale in the US, the company announced today.

The system automatically detects patient tube parameters, including sample identification, tube type, orders pending, and tube weight, within the first three seconds to help eliminate preanalytical errors.

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As cases of COVID-19 continued to grow this spring and summer in the US, so too did the number of Emergency Use Authorizations from the FDA for clinical diagnostic tests aimed at detecting current and past infections.