FDAnews Device Daily Bulletin

CEPHEID SUBMITS XPERT EV TEST FOR UNITED STATES REGULATORY APPROVAL

April 18, 2006
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Cepheid today submitted its Xpert EV (enterovirus) assay for use on the GeneXpert System to the FDA for regulatory clearance. Cepheid is seeking clearance of this assay as a laboratory test to aid in the detection of EV-associated meningitis.
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