Gauderer Gastrostomy Button

FDA 510(k) K843392 · American V. Mueller

Substantially Equivalent

510(k) numberK843392

Submission

Device name
Gauderer Gastrostomy Button
Applicant
American V. Mueller
Chicago, IL, US
Received
August 29, 1984
Decision date
October 11, 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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Questions and answers

When was Gauderer Gastrostomy Button cleared by the FDA?

Gauderer Gastrostomy Button (K843392) received a 510(k) decision of Substantially Equivalent on October 11, 1984, 43 days after the submission was received.

What is the product code of K843392?

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