# K925854: Vygon - Enteral Feeding Tube - Polyurethane

- Pathway: 510(k) (Traditional)
- Applicant: Vygon Corp.
- Decided: May 2, 1994 after 531 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.
9 later devices descend from it; 3 cite it directly.
0 of 10 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
- K020005: Infant Feeding Tubes (2002), 7 descendants of its own
- K052903: Pediatric Feeding Tube (2005), 6 descendants of its own
- K072756: Non-IV Adapter for Infant NG Tube (2007), 5 descendants of its own
- K082710: Safechild Enteral Feeding Tube and Accessories and Feeding Tube Extension Set (2009), 4 descendants of its own
- K092628: Enteral Feeding Tube and Accessories, Feeding Tube Extension Set (2010), 2 descendants of its own

Source page: https://510kreport.com/device/K925854
Methodology: https://510kreport.com/methodology