Lumipulse G ß-Amyloid Ratio (1-42/1-40) — Fujirebio Diagnostics,Inc. (510(k) DEN200072)
Lumipulse G ß-Amyloid Ratio (1-42/1-40) — Fujirebio Diagnostics,Inc. (510(k) DEN200072) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: Lumipulse G ß-Amyloid Ratio (1-42/1-40); Applicant: Fujirebio Diagnostics,Inc.; Clearance track: 510(k).
| Device name | Lumipulse G ß-Amyloid Ratio (1-42/1-40) |
|---|---|
| Applicant | Fujirebio Diagnostics,Inc. |
| Clearance track | 510(k) |
| Submission number | DEN200072 |
| Decision | Unknown |
| Decision date | 2022-05-04 |
| Date received | 2020-11-20 |
| Product code | QSE |
| Device class | 2 |
| Medical specialty | Immunology |
| Applicant location | PA, US |
| Source | openFDA device |
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