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QUICKVUE RSV - Quickvue Rsv (20 Test Kit), Model 20193
FDA 510(k)Class I (US FDA 510(k))
510(k) K061008
by Quidel Corp.
Identifiers
- 510(k) Number
- K061008 FDA 510(k)
- FDA Product Code
- MCE FDA 510(k)
- Models / Variants
- Quickvue Rsv (20 Test Kit), Model 20193 FDA 510(k)(2 Test Kit), Model 20199 FDA 510(k)
Classification
- Device Class
- Class I FDA 510(k)
- Legislation / Framework
- 21 CFR Part 866.3480 FDA 510(k)
- Regulation Number
- 866.3480 FDA 510(k)
- Advisory Committee
- Microbiology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
QUICKVUE RSV - Quickvue Rsv (20 Test Kit), Model 20193 by Quidel Corp. — Class I — FDA_510K — listed in FDA 510(k) — 2 models — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K061008 | Class I | Active |
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Manufacturer
- Manufacturer
- Quidel Corp.
Sources (1)
- FDA 510(k) K061008 24 fields · synced Jun 18, 2026