By a GenomeWeb staff reporter

NEW YORK (GenomeWeb News) – GenMark Diagnostics today said that it has filed with the US Food and Drug Administration for 510(k) clearance of its Respiratory Viral Panel.

The test would run on the firm's eSensor XT-8 and is designed to identify multiple viruses from patients exhibiting symptoms of respiratory infection. The Carlsbad, Calif.-based firm previously stated that the test would detect 21 upper respiratory viruses.

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In Science this week: mtDNA analysis give glimpse into decline of Neanderthals in Europe, and more.

The University of Arizona's Raina Maier writes that an understanding of the Earth's microbiome is needed.

The proposed Canadian budget emphasizes partnerships with industry, Nature News reports.

An Australian study of personalized medicine has run into problems as it recruits patients.

Apr
29
Sponsored by
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This online seminar will review case studies demonstrating the clinical utility of CTCs and cfDNA to define and characterize a variety of dynamic genomic changes throughout the course of cancer detection and treatment.