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2nd July 2019  Product update: Luminex Corporation

Luminex Submits ARIES MRSA Assay for FDA Clearance


Luminex Corporation has submitted the ARIES® MRSA Assay to the U.S. Food and Drug Administration (FDA) for clearance on Friday, June 28, 2019. The assay is a real-time, quantitative polymerase chain reaction (qPCR)-based, in vitro diagnostic test for the direct detection of methicillin-resistant Staphylococcus aureus (MRSA) DNA from nasal swabs in patients at risk for nasal colonization.

The Luminex ARIES® System is a sample to answer, real-time system designed to increase laboratory efficiency, ensure result accuracy, and fit seamlessly into the modern laboratory. The system already offers six FDA and seven CE-IVD cleared assays, as well as the ability to run laboratory developed tests.


    

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Date Published: 2nd July 2019

Source article link: https://www.prnewswire.com/news-releases/luminex-submits-aries-mrsa-assay-for-fda-clearance-300878870.html

Note: This content has been edited by a rapidmicrobiology staff writer for style and content.


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