Identifiers
- 510(k) Number
- K251139 FDA 510(k)
- FDA Product Code
- KPE FDA 510(k)
- Models / Variants
- KabiHelp® Uno FDA 510(k)KabiHelp® Advance plus FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 880.5025 FDA 510(k)
- Regulation Number
- 880.5025 FDA 510(k)
- Advisory Committee
- General Hospital FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
KabiHelp® Uno +1 more model by Fresenius Kabi AG — Class II — FDA_510K — listed in FDA 510(k) — 2 models — 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 | K251139 | Class II | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Fresenius Kabi AG
Sources (1)
- FDA 510(k) K251139 24 fields · synced Jun 19, 2026