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BioSieve™ Fentanyl FIA Test Kit +1 more model
FDA 510(k)Class II (US FDA 510(k))
510(k) K240124
Identifiers
- 510(k) Number
- K240124 FDA 510(k)
- FDA Product Code
- DJG FDA 510(k)
- Models / Variants
- BioSieve™ Fentanyl FIA Test Kit FDA 510(k)BioSieve™ ToxiSmart FIA Reader FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 862.3650 FDA 510(k)
- Regulation Number
- 862.3650 FDA 510(k)
- Advisory Committee
- Clinical Toxicology FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
BioSieve™ Fentanyl FIA Test Kit +1 more model by VivaChek Biotech (Hangzhou) Co., Ltd. — Class II — FDA_510K — listed in FDA 510(k) — 2 models
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 | K240124 | Class II | Active |
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Manufacturer
- Manufacturer
- VivaChek Biotech (Hangzhou) Co., Ltd.
Sources (1)
- FDA 510(k) K240124 24 fields · synced Jun 19, 2026