Jejunostomy Set for Tube Feeding

FDA 510(k) K841428 · Burron Medical Products, Inc.

Substantially Equivalent

510(k) numberK841428

Submission

Device name
Jejunostomy Set for Tube Feeding
Applicant
Burron Medical Products, Inc.
Mchenry, IL, US
Received
April 6, 1984
Decision date
July 9, 1984
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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K860126Stimuplex, Nerve StimulatorBXN · Traditional 02/28/1986SE
K851293ImplantofixLJT · Traditional 01/09/1986SE
K834383Dual-Lumen Long Term Central Venous CatLJS · Traditional 05/01/1984SE
K834299Long Term Central Venous Access CathLJS · Traditional 05/01/1984SE
K834473Multi-Lumen Central Venous Cath. KitLJS · Traditional 04/30/1984SE
K840179Continuous Epidural Anesthes. TrayCAZ · Traditional 02/24/1984SE
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Questions and answers

When was Jejunostomy Set for Tube Feeding cleared by the FDA?

Jejunostomy Set for Tube Feeding (K841428) received a 510(k) decision of Substantially Equivalent on July 9, 1984, 94 days after the submission was received.

What is the product code of K841428?

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