# Multi-Analyte Respiratory Virus Antigen Detection Test
> **Product code: SCA** · Class II — Moderate Risk (510(k) clearance required) · Microbiology · 21 CFR 866.3987
## Classification
- **FDA Product Code:** SCA
- **Device class:** Class II — Moderate Risk (510(k) clearance required)
- **Regulation:** 21 CFR 866.3987
- **Review panel:** MI
- **Medical specialty:** Microbiology
- **Submission type:** 1
- **GMP exempt:** N
- **Life sustaining:** N
- **Implant:** N
- **Third-party review:** N
## Definition

A multi-analyte respiratory virus antigen detection test is an in vitro diagnostic device intended for the detection and/or differentiation of respiratory viruses directly from respiratory clinical specimens. The device is intended to be performed at the site of sample collection, does not involve sample storage and/or transport.

## Market data
- **Cleared 510(k) submissions:** 11
- **Registered establishments:** 20
## Source
- [FDA Device Classification](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classification.cfm?ID=SCA)
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