Dimix Container for Parneteral Nutrit

FDA 510(k) K840915 · Gil-Med Industries C/O Kegan & Kegan, Ltd.

Substantially Equivalent

510(k) numberK840915

Submission

Device name
Dimix Container for Parneteral Nutrit
Applicant
Gil-Med Industries C/O Kegan & Kegan, Ltd.
Mchenry, IL, US
Received
February 29, 1984
Decision date
April 17, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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
K210749Empty EVA BagKPE · Traditional Haemotronic S.P.A.08/19/2021SE
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More from Gilero, LLC

510(k)DeviceDecision
K880506Modified Eva-Mix and Di-Mix BagsKPE · Traditional 05/20/1988SE
K870274Di-Mix Parenteral Nutrition & Medicine ContainerKPE · Traditional 02/10/1987SE
K861862Dieto Container for Enteral NutritionKNT · Traditional 08/11/1986SE
K841597Gil-Med Parenteral Nutrition or MedicineKPE · Traditional 10/26/1984SE
K841224Uro-Male Incontinence CatheterKNX · Traditional 05/02/1984SE
K840916Dieto Container for Enternal NutritKNT · Traditional 04/04/1984SE

Questions and answers

When was Dimix Container for Parneteral Nutrit cleared by the FDA?

Dimix Container for Parneteral Nutrit (K840915) received a 510(k) decision of Substantially Equivalent on April 17, 1984, 48 days after the submission was received.

What is the product code of K840915?

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