Xro Gastro-Duodenal, Dual Flow Tube, Salem Type

FDA 510(k) K860285 · Vygon Corp.

Substantially Equivalent

510(k) numberK860285

Submission

Device name
Xro Gastro-Duodenal, Dual Flow Tube, Salem Type
Applicant
Vygon Corp.
East Rutherford, NJ, US
Received
January 28, 1986
Decision date
February 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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Questions and answers

When was Xro Gastro-Duodenal, Dual Flow Tube, Salem Type cleared by the FDA?

Xro Gastro-Duodenal, Dual Flow Tube, Salem Type (K860285) received a 510(k) decision of Substantially Equivalent on February 11, 1986, 14 days after the submission was received.

What is the product code of K860285?

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