By a GenomeWeb staff reporter

NEW YORK (GenomeWeb News) – Luminex said after the close of the market on Tuesday that the US Food and Drug Administration has given 510(k) clearance for its xTag Respiratory Viral Panel Fast.

The panel includes respiratory syncytial virus; influenza A; non-specific influenza A; H1 subtype; H3 subtype; influenza B; metapneumovirus; adenovirus; and entero-rhinovirus.

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