# K920703: Gastrointestinal Feeding Tube

- Pathway: 510(k) (Traditional)
- Applicant: Wilson-Cook Medical, Inc.
- Decided: Dec 3, 1993 after 654 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.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K183336: Entuit PEG, Entuit PEGJ (2019), 2 descendants of its own
- K213356: Entuit PEG, Entuit PEGJ (2022), 1 descendant of its own
- K254170: Percutaneous Endoscopic Gastrostomy (PEG) Kit (2026), 0 descendants of its own

## Recalls of this device
- Jul 24, 2009 · Not classified · Z-1910-2009: The English only version of the Patient Care Manuals that accompany the device were shipped to a medical facility in Italy.

Source page: https://510kreport.com/device/K920703
Methodology: https://510kreport.com/methodology