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U.S. Department of Health and Human Services

Product Classification

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Device over-the-counter molecular multi-analyte respiratory virus detection test
Definition An over-the-counter molecular multi-analyte respiratory virus detection test is an in vitro diagnostic device for the detection and/or differentiation of respiratory viruses directly from clinical specimens. The device is intended to be used by lay users and without health care provider (HCP) intervention in home settings or similar environments.
Physical State In vitro diagnostic assay reagents and hardware. The device may include chemical components for the amplification of nucleic acid targets. The device may include hardware and software to allow for data collection and review.
Technical Method Uses nucleic acid amplification technology (NAAT) for the detection of respiratory viruses from clinical samples.
Target Area upper respiratory clinical specimens
Regulation Medical Specialty Microbiology
Review Panel Microbiology
Product CodeSIA
Premarket Review Office of In Vitro Diagnostics (OHT7)
Division of Microbiology Devices (DMD)
Submission Type 510(k)
Regulation Number 866.3984
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting
Ineligible
Implanted Device? No
Life-Sustain/Support Device? No
Third Party Review Not Third Party Eligible
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