IV Trifurcated Extension Set
FDA 510(k) K900427 · Marquette Medical, Inc.
510(k) numberK900427
Submission
- Device name
- IV Trifurcated Extension Set
- Applicant
- Marquette Medical, Inc.
Crofton, MD, US - Received
- January 30, 1990
- Decision date
- February 28, 1990
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- FPA – Set, Administration, Intravascular
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.5440
- Specialty
- General Hospital
Other 510(k)s with product code FPA
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| 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 |
|---|---|---|
| K021471 | Marquette Huber Trap Safety Infusion SetFPA · Traditional | 09/08/2003SE |
| K953008 | Infant Feeding TubeFPD · Traditional | 01/11/1996SE |
| K952976 | Plastic Blunt CannulaFPA · Traditional | 09/15/1995SE |
| K920537 | Subcutaneous Infusion SetFPA · Traditional | 10/13/1992SE |
| K905219 | 4' Low Volume IV Extension SetFPA · Traditional | 06/04/1991SE |
| K905218 | 4 Low Volume IV Extension Set with Slide ClampFPA · Traditional | 06/04/1991SE |
| K905374 | IV Extension Sets with .22 Micron FilterFPA · Traditional | 05/31/1991SE |
| K901089 | Low Volume Trifurcated IV Extension SetFPA · Traditional | 10/04/1990SE |
| K901088 | Low Volume Bifurcated IV Extension SetFPA · Traditional | 10/04/1990SE |
| K900426 | IV Bifurcated Extension SetFPA · Traditional | 02/28/1990SE |
Questions and answers
When was IV Trifurcated Extension Set cleared by the FDA?
IV Trifurcated Extension Set (K900427) received a 510(k) decision of Substantially Equivalent on February 28, 1990, 29 days after the submission was received.
What is the product code of K900427?
The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.