KabiHelp® Uno; KabiHelp® Advance plus
FDA 510(k) K251139 · Fresenius Kabi AG
510(k) numberK251139
Submission
- Device name
- KabiHelp® Uno; KabiHelp® Advance plus
- Applicant
- Fresenius Kabi AG
Bad Homburg, DE - Received
- April 14, 2025
- Decision date
- January 9, 2026
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KPE – Container, I.V.
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5025
- Specialty
- General Hospital
Other 510(k)s with product code KPE
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K252079 | Disposable Infusion Bag for Parenteral NutritionKPE · Traditional | Beijing L&Z Medical Technology Development Co.… | 04/02/2026SE |
| K251980 | ClaveQS BagKPE · Traditional | Icu Medical, Inc. | 03/20/2026SE |
| K252094 | eZSURE Empty Fluid ContainerKPE · Special | Epic Medical Pte. , Ltd. | 08/01/2025SE |
| K250459 | DMRX 100ml Empty Container Solution; DMRX 250ml Empty Container Solution; DMRX 500ml…KPE · Traditional | Technoflex Sas. | 04/18/2025SE |
| K241442 | eZSURE Empty Fluid Container with ProSeal Injection SiteKPE · Special | Epic Medical Pte. , Ltd. | 06/21/2024SE |
| K223674 | eZSURE Empty Fluid Container (models 426030, 426040, 426110)KPE · Traditional | Epic Medical Pte. , Ltd. | 09/01/2023SE |
| K222622 | Disposable Infusion Bag for Parenteral NutritionKPE · Traditional | Beijing L&Z Medical Technology Development Co.… | 02/16/2023SE |
| K210749 | Empty EVA BagKPE · Traditional | Haemotronic S.P.A. | 08/19/2021SE |
| K201936 | SmartSite Bag 500mL, SmartSite Bag 250 mL, SmartSite Bag 100 mLKPE · Traditional | Gilero, LLC | 05/06/2021SE |
| K193528 | Empty EVA BagKPE · Traditional | Haemotronic S.P.A. | 07/22/2020SE |
More from Haemotronic S.P.A.
| 510(k) | Device | Decision |
|---|---|---|
| K221121 | Volumat Polyethylene I.V. Administration SetFPA · Traditional | 06/16/2023SE |
| K220301 | Volumat LineFPA · Traditional | 06/02/2023SE |
| K212445 | freeflex+ Transfer AdapterLHI · Traditional | 06/01/2022SE |
| K210075 | Vigilant Software Suite Vigilant Master MedPHC · Traditional | 03/01/2022SE |
| K210074 | Agilia SP Infusion System, Agilia SP MC WIFI Infusion Pump, Agilia Link, Agilia Duo…FRN · Traditional | 03/01/2022SE |
| K210073 | Agilia VP Infusion System, Agilia VP MC WIFI Infusion Pump, Volumat Lines Administration…FRN · Traditional | 03/01/2022SE |
| K210089 | CATSmart, Automated Blood Processing Autotransfusion SystemCAC · Special | 02/11/2021SE |
| K200530 | AMICUS Separator SystemGKT · Traditional | 09/11/2020SE |
| K192150 | AMICUS Separator SystemLKN · Traditional | 11/13/2019SE |
| K192368 | CATSmartCAC · Special | 09/27/2019SE |
Questions and answers
When was KabiHelp® Uno; KabiHelp® Advance plus cleared by the FDA?
KabiHelp® Uno; KabiHelp® Advance plus (K251139) received a 510(k) decision of Substantially Equivalent on January 9, 2026, 270 days after the submission was received.
What is the product code of K251139?
The FDA product code is KPE – Container, I.V., a Class II (moderate risk) device regulated under 21 CFR 880.5025.