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BioSieve Multi-Drug Urine Test Panel - BioSieve Multi-Drug Urine Home Test Panel
FDA 510(k)Class II (US FDA 510(k))
510(k) K261280
Identifiers
- 510(k) Number
- K261280 FDA 510(k)
- FDA Product Code
- NFT FDA 510(k)
- Models / Variants
- BioSieve Multi-Drug Urine Test Panel FDA 510(k)BioSieve Multi-Drug Urine Home Test Panel FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 862.3100 FDA 510(k)
- Regulation Number
- 862.3100 FDA 510(k)
- Advisory Committee
- Clinical Toxicology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
BioSieve Multi-Drug Urine Test Panel - BioSieve Multi-Drug Urine Home Test Panel by VivaChek Biotech (Hangzhou) Co., Ltd. — Class II — FDA_510K — listed in…
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 | K261280 | Class II | Active |
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Manufacturer
- Manufacturer
- VivaChek Biotech (Hangzhou) Co., Ltd.
Sources (1)
- FDA 510(k) K261280 24 fields · synced Jun 18, 2026