Omnimed IV Solution Administration Set
FDA 510(k) K850112 · Omni Intl., Inc.
510(k) numberK850112
Submission
- Device name
- Omnimed IV Solution Administration Set
- Applicant
- Omni Intl., Inc.
Palm Springs, CA, US - Received
- January 14, 1985
- Decision date
- February 22, 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 |
|---|---|---|
| K984066 | Omnigrip, Latex Surgical Glove, Powder-Free with Protein Labeling ClaimKGO · Traditional | 01/13/1999SE |
| K984064 | Omnigrip, Latex Surgical Glove, Powder FreeKGO · Traditional | 01/08/1999SE |
| K853255 | Omnimed I.V. Solution Admin. SetFPA · Traditional | 08/23/1985SE |
| K851938 | Omnimed Surgical GownFYA · Traditional | 06/28/1985SE |
| K851654 | Omnimed ClampHXD · Traditional | 05/31/1985SE |
| K851734 | Omnimed Superior Transducer ProtectorFIB · Traditional | 05/23/1985SE |
| K850706 | F-Series ImplantDZE · Traditional | 04/10/1985SE |
| K850066 | Omnimed Nasal Oxygen CannulaCAT · Traditional | 01/24/1985SE |
| K831147 | Omniprobe Electrical Nerve StimulatorGZJ · Traditional | 07/18/1983SE |
| K821523 | Omni TENSGZJ · Traditional | 06/16/1982SE |
Questions and answers
When was Omnimed IV Solution Administration Set cleared by the FDA?
Omnimed IV Solution Administration Set (K850112) received a 510(k) decision of Substantially Equivalent on February 22, 1985, 39 days after the submission was received.
What is the product code of K850112?
The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.