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www.fdanews.com/articles/86122-cepheid-submits-xpert-ev-test-for-united-states-regulatory-approval

CEPHEID SUBMITS XPERT EV TEST FOR UNITED STATES REGULATORY APPROVAL

April 17, 2006

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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