eZSURE™ Empty Fluid Container with ProSeal™ Injection Site

FDA 510(k) K241442 · Epic Medical Pte. , Ltd.

Substantially Equivalent

510(k) numberK241442

Submission

Device name
eZSURE™ Empty Fluid Container with ProSeal™ Injection Site
Applicant
Epic Medical Pte. , Ltd.
Singapore, SG
Received
May 22, 2024
Decision date
June 21, 2024
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KPE – Container, I.V.
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5025
Specialty
General Hospital

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K222622Disposable Infusion Bag for Parenteral NutritionKPE · Traditional Beijing L&Z Medical Technology Development Co.…02/16/2023SE
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More from Haemotronic S.P.A.

510(k)DeviceDecision
K252987ADRx™ Admixture DeviceLHI · Traditional 06/12/2026SE
K250234SMARTeZ™ Elastomeric Infusion Pump (RS series)MEB · Traditional 04/24/2026SE
K251722ProSeal™ Transfer Injector (421120, 421130, 421140)ONB · Special 12/05/2025SE
K251814EZ™ IV Administration SetFPA · Traditional 08/29/2025SE
K252094eZSURE™ Empty Fluid ContainerKPE · Special 08/01/2025SE
K251340ProSeal™ Bag Spike with Additive Port (423370ST, 423370)ONB · Special 05/29/2025SE
K243976ZeroClear™ Bag Access (423100)ONB · Special 01/22/2025SE
K240517ProSeal™ Vented Universal Vial AdaptorONB · Traditional 12/26/2024SE
K241988ProSeal™ Closed System Bag AccessONB · Traditional 10/23/2024SE
K241735ProSeal™ In Line Pump Set (423850)ONB · Special 10/10/2024SE

Questions and answers

When was eZSURE™ Empty Fluid Container with ProSeal™ Injection Site cleared by the FDA?

eZSURE™ Empty Fluid Container with ProSeal™ Injection Site (K241442) received a 510(k) decision of Substantially Equivalent on June 21, 2024, 30 days after the submission was received.

What is the product code of K241442?

The FDA product code is KPE – Container, I.V., a Class II (moderate risk) device regulated under 21 CFR 880.5025.