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FDA 510(k)

Traditional Length GJ Feeding Device

K-Number: K182804 · 2019-03-01

Decision Date2019-03-01
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Traditional Length GJ Feeding Device is a medical device manufactured by Applied Medical Technology, Inc.. It received FDA 510(k) clearance on 2019-03-01 under approval number K182804. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Traditional Length GJ Feeding Device?

Traditional Length GJ Feeding Device is a medical device that received FDA 510(k) clearance on 2019-03-01. It is manufactured by Applied Medical Technology, Inc.. The 510(k) number is K182804.

When was Traditional Length GJ Feeding Device approved by the FDA?

Traditional Length GJ Feeding Device received FDA 510(k) clearance on 2019-03-01, under approval number K182804.

What company makes Traditional Length GJ Feeding Device?

Traditional Length GJ Feeding Device is manufactured by Applied Medical Technology, Inc..

What is the FDA product code for Traditional Length GJ Feeding Device?

The FDA product code for Traditional Length GJ Feeding Device is KNT.

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Official Source

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