Sub-Q Subcutaneous Tissue Infusion Set
FDA 510(k) K140131 · Emed Technologies Corporation
510(k) numberK140131
Submission
- Device name
- Sub-Q Subcutaneous Tissue Infusion Set
- Applicant
- Emed Technologies Corporation
El Dorado Hills, CA, US - Received
- January 17, 2014
- Decision date
- April 3, 2014
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary 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 |
|---|---|---|
| K251105 | Tetra (TM-20); Tetra (TM-50)PKP · Traditional | 12/22/2025SE |
| K240148 | SCIg60 Infusion SystemPKP · Special | 02/16/2024SE |
| K230883 | VersaPump Infusion SystemPKP · Traditional | 11/28/2023SE |
| K213429 | AccuSert Needle InserterKZH · Traditional | 10/20/2022SE |
| K222087 | SCIg60 Infusion SystemPKP · Traditional | 10/13/2022SE |
| K173783 | SCIg60 Infusion SystemPKP · Traditional | 12/14/2018SE |
| K161906 | SCIg60 InfuserPKP · Traditional | 12/01/2016SE |
| K142319 | SCIg60 Infuser, InfusetPKP · Traditional | 05/14/2015SE |
| K140133 | Infuset Flow Control Extension SetFPA · Traditional | 05/15/2014SE |
| K123729 | Versarate Flow Rate ControlerFPA · Traditional | 12/21/2012SE |
Questions and answers
When was Sub-Q Subcutaneous Tissue Infusion Set cleared by the FDA?
Sub-Q Subcutaneous Tissue Infusion Set (K140131) received a 510(k) decision of Substantially Equivalent on April 3, 2014, 76 days after the submission was received.
What is the product code of K140131?
The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.