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U.S. Department of Health and Human Services

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Device non-sars coronavirus multiplex nucleic acid assay
Regulation Description Respiratory viral panel multiplex nucleic acid assay.
Definition A non-sars coronavirus multiplex nucleic acid assay is a multiplex in vitro diagnostic test for the simultaneous qualitative detection and discrimination of coronavirus 229e, coronavirus nl63, coronavirus hku1 and coronavirus oc43 nucleic acids isolated and purified from human respiratory specimens obtained from individuals exhibiting signs and symptoms of respiratory tract infections or viral culture.The detection and discrimination of human non-sars coronavirus nucleic acids from symptomatic patients aid in the diagnosis of human respiratory tract non-sars coronavirus infections if used in conjunction with other clinical and laboratory findings.
Physical State Nucleic Acid Based Assay
Technical Method Multiplex nucleic acid assay
Target Area IVD
Regulation Medical Specialty Microbiology
Review Panel Microbiology
Product CodeOTG
Premarket Review Office of In Vitro Diagnostics and Radiological Health (OIR)
Submission Type 510(k)
Regulation Number 866.3980
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Third Party Review Not Third Party Eligible
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