C-Series Homepump
FDA 510(k) K944692 · Block Medical, Inc.
510(k) numberK944692
Submission
- Device name
- C-Series Homepump
- Applicant
- Block Medical, Inc.
Carlsbad, CA, US - Received
- September 23, 1994
- Decision date
- May 2, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 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
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 |
|---|---|---|
| K940117 | MID-500MEB · Traditional | 06/10/1994ST |
| K934551 | Verifuse Ambulatory PumpMEA · Traditional | 03/17/1994SE |
| K935236 | Flow Controlling Extension SetLDR · Traditional | 02/24/1994SE |
| K932740 | Homepump NSFMED · Traditional | 10/06/1993SE |
| K904663 | Auto Sash (TM)FPA · Traditional | 11/23/1992SE |
| K914924 | Chemo Priming Pin(Tm)FPA · Traditional | 03/06/1992SE |
| K914855 | Multiple Dose ControllerFRN · Traditional | 01/24/1992SE |
| K914854 | ThumperFRN · Traditional | 01/24/1992SE |
| K910695 | Auto Sash (TM)FPA · Traditional | 03/21/1991SE |
| K902891 | Verifuse Ambulatory PumpFRN · Traditional | 11/21/1990SE |
Questions and answers
When was C-Series Homepump cleared by the FDA?
C-Series Homepump (K944692) received a 510(k) decision of Substantially Equivalent on May 2, 1995, 221 days after the submission was received.
What is the product code of K944692?
The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.