Dieto Container for Enteral Nutrition

FDA 510(k) K861862 · Gil-Med Industries C/O Kegan & Kegan, Ltd.

Substantially Equivalent

510(k) numberK861862

Submission

Device name
Dieto Container for Enteral Nutrition
Applicant
Gil-Med Industries C/O Kegan & Kegan, Ltd.
Chicago, IL, US
Received
May 13, 1986
Decision date
August 11, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KNT – Tubes, Gastrointestinal (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5980
Specialty
Gastroenterology, Urology

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More from Degania Silicone , Ltd.

510(k)DeviceDecision
K880506Modified Eva-Mix and Di-Mix BagsKPE · Traditional 05/20/1988SE
K870274Di-Mix Parenteral Nutrition & Medicine ContainerKPE · Traditional 02/10/1987SE
K841597Gil-Med Parenteral Nutrition or MedicineKPE · Traditional 10/26/1984SE
K841224Uro-Male Incontinence CatheterKNX · Traditional 05/02/1984SE
K840915Dimix Container for Parneteral NutritKPE · Traditional 04/17/1984SE
K840916Dieto Container for Enternal NutritKNT · Traditional 04/04/1984SE

Questions and answers

When was Dieto Container for Enteral Nutrition cleared by the FDA?

Dieto Container for Enteral Nutrition (K861862) received a 510(k) decision of Substantially Equivalent on August 11, 1986, 90 days after the submission was received.

What is the product code of K861862?

The FDA product code is KNT – Tubes, Gastrointestinal (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 876.5980.