← Back to catalogue
Lumipulse G ß-Amyloid Ratio (1-42/1-40)
FDA 510(k)Class II (US FDA 510(k))
510(k) DEN200072
Identifiers
- 510(k) Number
- DEN200072 FDA 510(k)
- FDA Product Code
- QSE FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 866.5840 FDA 510(k)
- Regulation Number
- 866.5840 FDA 510(k)
- Advisory Committee
- Immunology FDA 510(k)
- FDA Decision
- DENG FDA 510(k)
Lumipulse G ß-Amyloid Ratio (1-42/1-40) by Fujirebio Diagnostics, Inc. — Class II — FDA_510K — listed in FDA 510(k) — 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 | DEN200072 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Fujirebio Diagnostics, Inc.
- FDA Applicant
- Fujirebio Diagnostics,Inc.
Sources (1)
- FDA 510(k) DEN200072 24 fields · synced Jun 18, 2026