# K123716: Amt Low-Profile Transgastric-Jejunal Feeding Tube Kit

- Pathway: 510(k) (Traditional)
- Applicant: Applied Medical Technology, Inc.
- Decided: Apr 19, 2013 after 136 days
- Product code: KNT (Tubes, Gastrointestinal (And Accessories))
- Device class: 2
- Regulation: 21 CFR 876.5980
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K183508: Micro Transgastric-Jejunal Feeding Device (2019), 0 descendants of its own
- K182804: Traditional Length GJ Feeding Device (2019), 0 descendants of its own

## Recalls of this device
- Jan 26, 2016 · Class II · Z-1497-2016: The firm received complaints that the product is shorter in length than indicated on the label.

## Indications for use
The AMT Transgastric-Jejunal feeding tube is indicated for use in patients who cannot absorb adequate nutrition through the stomach, who have intestinal motility problems, gastric outlet obstruction, severe gastroesophageal reflux, are at risk of aspiration, or in those who have had previous esophagectomy or gastrectomy. The use of this tube is also clinically indicated when simultaneous gastric decompression and jejunal feeding are needed. This includes patients in whom malnutrition already exists, or may result, secondary to concurrent conditions.

Source page: https://510kreport.com/device/K123716
Methodology: https://510kreport.com/methodology