Dynafeed Enteral Pump Feed Bag

FDA 510(k) K860075 · Medline Industries, Inc.

Substantially Equivalent

510(k) numberK860075

Submission

Device name
Dynafeed Enteral Pump Feed Bag
Applicant
Medline Industries, Inc.
Mundelein, IL, US
Received
January 7, 1986
Decision date
January 23, 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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Questions and answers

When was Dynafeed Enteral Pump Feed Bag cleared by the FDA?

Dynafeed Enteral Pump Feed Bag (K860075) received a 510(k) decision of Substantially Equivalent on January 23, 1986, 16 days after the submission was received.

What is the product code of K860075?

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