# K070124: Gastrostomy Replacement Tube, Model 253

- Pathway: 510(k) (Traditional)
- Applicant: Degania Silicone, Ltd.
- Decided: May 23, 2007 after 127 days
- Product code: KNT (Tubes, Gastrointestinal (And Accessories))
- Device class: 2
- Regulation: 21 CFR 876.5980
- Recalls of this device: none
- 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; 1 cites 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
- K143378: AQUARIUS Gastrostomy Replacement Tube (2014), 1 descendant of its own
- K180622: Kangaroo Gastrostomy Feeding Tube with ENFit Y-Port (2018), 0 descendants of its own

## Indications for use
Gastrostomy Replacement Tube of Degania Silicone Ltd is indicated for use in a well established Gastrostomy tract for feeding and/or administration of medication. May be used for gastric decompression.

Source page: https://510kreport.com/device/K070124
Methodology: https://510kreport.com/methodology