Subcutaneous Infusion Set
FDA 510(k) K932637 · Douglas Medical Products Corp.
510(k) numberK932637
Submission
- Device name
- Subcutaneous Infusion Set
- Applicant
- Douglas Medical Products Corp.
Mundelein, IL, US - Received
- June 2, 1993
- Decision date
- January 7, 1994
- 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
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 |
|---|---|---|
| K162951 | TUBETECH IV Administration SetFPA · Traditional | 07/28/2017SE |
| K961155 | Solo Picc/Midline Catheter Kit Models 71924, 71908LJS · Traditional | 06/18/1996SE |
| K954428 | Solopicc 24 (60CM) 20GA CatheterFOZ · Traditional | 03/28/1996SE |
| K941628 | 40 Micron Blood Transfusion FilterFPB · Traditional | 02/16/1995SE |
| K942101 | 4-LEAD Irrigation SetHRX · Traditional | 09/30/1994SE |
| K941453 | Check Valve Solution SetFPA · Traditional | 08/16/1994SE |
| K930854 | Solution Set with .2 Micron FilterFPA · Traditional | 01/14/1994SE |
| K931659 | 3 Lead ConnectorFPA · Traditional | 01/07/1994SE |
| K931658 | In-Line Burette SetFPA · Traditional | 12/21/1993SE |
| K932638 | Huber Needle Infusion SetFPA · Traditional | 12/14/1993SE |
Questions and answers
When was Subcutaneous Infusion Set cleared by the FDA?
Subcutaneous Infusion Set (K932637) received a 510(k) decision of Substantially Equivalent on January 7, 1994, 219 days after the submission was received.
What is the product code of K932637?
The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.