December 22, 2016 / 1:18 PM / 9 months ago

BRIEF-GenMark Diagnostics submits 510(k) applications to the FDA

Dec 22 (Reuters) - Genmark Diagnostics Inc :

* Genmark Diagnostics Inc - expect blood culture id family of panels to be available in Europe during q1 of 2017

* Genmark Diagnostics submits 510(k) applications to the FDA for eplex sample-to-answer instrument and respiratory pathogen panel Source text for Eikon: Further company coverage:

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