
Luminex Corporation
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ARIES Group A Strep Assay, ARIES Group A Strep Assay Protocol File Kit is an FDA 510(k)-cleared medical device (K172402) manufactured by Luminex Corporation. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 29, 2017. Regulation: 8.

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