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APDN Receives FDA Emergency Use Authorization for COVID-19 Diagnostic Assay Kit

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By HospiMedica International staff writers

Applied DNA Sciences Inc. (Stony Brook, NY, USA) has been granted Emergency Use Authorization (EUA) by the US Food and Drug Administration (FDA) for the clinical use of the company’s patent-pending Linea COVID-19 RT-PCR test.

The Linea COVID-19 assay kit is an rRT-PCR (reverse transcription, Real Time Polymerase Chain Reaction)-based assay designed to detect specific highly conserved target sequences of the SARS-CoV-2 Spike (S) gene.


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Assay kit | Coronavirus | EUA | FDA | HospiMedica | LinearDNA