Arrow Needle-Catheter Jejunostomy Kit

FDA 510(k) K810979 · Arrow Intl., Inc.

Substantially Equivalent

510(k) numberK810979

Submission

Device name
Arrow Needle-Catheter Jejunostomy Kit
Applicant
Arrow Intl., Inc.
Mchenry, IL, US
Received
April 10, 1981
Decision date
June 2, 1981
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 Arrow Needle-Catheter Jejunostomy Kit cleared by the FDA?

Arrow Needle-Catheter Jejunostomy Kit (K810979) received a 510(k) decision of Substantially Equivalent on June 2, 1981, 53 days after the submission was received.

What is the product code of K810979?

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