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BioFire Diagnostics, Inc Submits 510(k) Application To FDA For FilmArray® Gastrointestinal Panel


2/19/2014 9:11:34 AM

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SALT LAKE CITY--(BUSINESS WIRE)--BioFire Diagnostics, LLC today announced that it has submitted the FilmArray Gastrointestinal (GI) Panel to the U.S. Food and Drug Administration (FDA) for 510(k) clearance. The comprehensive FilmArray GI Panel tests for over 20 common bacteria, viruses and parasites that cause infectious diarrhea.

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