I.V. Administration Set
FDA 510(k) K852106 · Mediflex Intl.
510(k) numberK852106
Submission
- Device name
- I.V. Administration Set
- Applicant
- Mediflex Intl.
Fairfield, NJ, US - Received
- May 15, 1985
- Decision date
- June 7, 1985
- 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 |
|---|---|---|
| K915140 | Primary Dressing TrayLYY · Traditional | 02/11/1992SEKD |
| K900841 | Hemodialysis Transducer ProtectorFIB · Traditional | 05/15/1990SE |
| K891077 | Mediverse Parenteral Nutrition BagKPE · Traditional | 05/24/1989SE |
| K884243 | Blood Tubing SetFJK · Traditional | 12/08/1988SE |
| K863496 | Mediflex Transducer ProtectorFIB · Traditional | 09/23/1986SE |
| K855039 | Mediflex Injection CapGCE · Traditional | 01/24/1986SE |
| K854346 | Mediflex Disposable Tubing ClampFPA · Traditional | 11/18/1985SE |
| K843126 | Mediflex Drainage BagKNX · Traditional | 10/04/1984SE |
Questions and answers
When was I.V. Administration Set cleared by the FDA?
I.V. Administration Set (K852106) received a 510(k) decision of Substantially Equivalent on June 7, 1985, 23 days after the submission was received.
What is the product code of K852106?
The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.