Ecomed Disposable Administration Sets

FDA 510(k) K234129 · Ecomed Solutions, LLC

Substantially Equivalent

510(k) numberK234129

Submission

Device name
Ecomed Disposable Administration Sets
Applicant
Ecomed Solutions, LLC
Mundelein, IL, US
Received
December 28, 2023
Decision date
September 20, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

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)DeviceApplicantDecision
K254123Ecomed Disposable Administration SetsFPA · Abbreviated Ecomed Solutions, LLC09/11/2026SE
K261530iiSure Infusion SetFPA · Special Deka Research and Development06/03/2026SE
K252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072…FPA · Traditional Amsino International, Inc.05/04/2026SE
K251375PuraCath Firefly Needleless Connector IT (9005)FPA · Traditional Puracath Medical, Inc.02/12/2026SE
K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free…FPA · Traditional Np Medical12/04/2025SE
K250325BD Alaris Pump Infusion SetFPA · Traditional Carefusion (Bd)10/30/2025SE
K251814EZ™ IV Administration SetFPA · Traditional Epic Medical Pte. , Ltd.08/29/2025SE
K251854SteadiSet infusion setFPA · Abbreviated Tandem Diabetes Care08/06/2025SE
K243841Sparta Infusion Set for InsulinFPA · Traditional Deka Research and Development08/01/2025SE
K243392Infusomat® Space Volumetric Infusion Pump Administration SetsFPA · Traditional B.Braun Medical, Inc.07/24/2025SE

More from B.Braun Medical, Inc.

510(k)DeviceDecision
K254123Ecomed Disposable Administration SetsFPA · Abbreviated 09/11/2026SE
K162088Ecomed Disposable Angiographic SyringesDXT · Traditional 01/27/2017SE

Questions and answers

When was Ecomed Disposable Administration Sets cleared by the FDA?

Ecomed Disposable Administration Sets (K234129) received a 510(k) decision of Substantially Equivalent on September 20, 2024, 267 days after the submission was received.

What is the product code of K234129?

The FDA product code is FPA – Set, Administration, Intravascular, a Class II (moderate risk) device regulated under 21 CFR 880.5440.