I.V. Priming Set
FDA 510(k) K913333 · Gainor Medical Europe, Ltd.
510(k) numberK913333
Submission
- Device name
- I.V. Priming Set
- Applicant
- Gainor Medical Europe, Ltd.
Mcdonough, GA, US - Received
- July 26, 1991
- Decision date
- October 23, 1991
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- FPA – Set, Administration, Intravascular
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5440
- Specialty
- General Hospital
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|---|---|---|---|
| K254123 | Ecomed Disposable Administration SetsFPA · Abbreviated | Ecomed Solutions, LLC | 09/11/2026SE |
| K261530 | iiSure Infusion SetFPA · Special | Deka Research and Development | 06/03/2026SE |
| K252543 | AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072…FPA · Traditional | Amsino International, Inc. | 05/04/2026SE |
| K251375 | PuraCath Firefly Needleless Connector IT (9005)FPA · Traditional | Puracath Medical, Inc. | 02/12/2026SE |
| K251257 | nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free…FPA · Traditional | Np Medical | 12/04/2025SE |
| K250325 | BD Alaris Pump Infusion SetFPA · Traditional | Carefusion (Bd) | 10/30/2025SE |
| K251814 | EZ IV Administration SetFPA · Traditional | Epic Medical Pte. , Ltd. | 08/29/2025SE |
| K251854 | SteadiSet infusion setFPA · Abbreviated | Tandem Diabetes Care | 08/06/2025SE |
| K243841 | Sparta Infusion Set for InsulinFPA · Traditional | Deka Research and Development | 08/01/2025SE |
| K243392 | Infusomat® Space Volumetric Infusion Pump Administration SetsFPA · Traditional | B.Braun Medical, Inc. | 07/24/2025SE |
More from B.Braun Medical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K926448 | I.V. Administration SetFPA · Traditional | 05/02/1994SE |
| K931828 | Carelet Safety LancetFMK · Traditional | 10/15/1993SE |
| K931827 | Cleanlet, Cleanlet XL & KidsFMK · Traditional | 09/13/1993SE |
| K922441 | Sureseal BandageKGX · Traditional | 08/10/1993SE |
| K902422 | Needle, Aspiration & Injection, DisposableFMI · Traditional | 06/06/1991SE |
| K902420 | Catheter, Nasal, OxygenCAT · Traditional | 04/17/1991SE |
| K902564 | Needle, DialysisFIE · Traditional | 03/01/1991SE |
| K902426 | Hemodialysis System and AccessoryFJK · Traditional | 11/20/1990SE |
| K902421 | Stomach, Gastro-EnterostomyKDH · Traditional | 11/20/1990SE |
| K902416 | Surelite and Surelite XL Blood LancetFMK · Traditional | 08/01/1990SE |
Questions and answers
When was I.V. Priming Set cleared by the FDA?
I.V. Priming Set (K913333) received a 510(k) decision of Substantially Equivalent on October 23, 1991, 89 days after the submission was received.
What is the product code of K913333?
The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.