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Fore V10 Blood Glucose Monitoring System (Td-4244 +2 more)
FDA 510(k)Class II (US FDA 510(k))
510(k) K090404
Identifiers
- 510(k) Number
- K090404 FDA 510(k)
- FDA Product Code
- NBW FDA 510(k)
- Models / Variants
- Td-4244 FDA 510(k)Forea V12 Blodo Glucose Monitoring System FDA 510(k)Model Td-4247 FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 862.1345 FDA 510(k)
- Regulation Number
- 862.1345 FDA 510(k)
- Advisory Committee
- Clinical Chemistry FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Fore V10 Blood Glucose Monitoring System (Td-4244 +2 more) by Taidoc Technology Corporation — Class II — FDA_510K — listed in FDA 510(k) — 3 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 | K090404 | Class II | Active |
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Manufacturer
- Manufacturer
- Taidoc Technology Corporation
Sources (1)
- FDA 510(k) K090404 24 fields · synced Jun 19, 2026