# K183336: Entuit PEG, Entuit PEGJ

- Pathway: 510(k) (Traditional)
- Applicant: Wilson-Cook Medical, Inc.
- Decided: May 29, 2019 after 177 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
Longest line of descent: 1 generation back to K920703 (1993). 1 ancestor in all.
2 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)
- K920703: Gastrointestinal Feeding Tube, Wilson-Cook Medical, Inc. (1993) Summary page 4.

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

## Indications for use
The Entuit PEG is intended for percutaneous endoscopic gastrostomy placement to provide enteral nutrition and/or medication to patients requiring nutritional support, and gastric decompression. This device is indicated for adult use only. The Entuit PEGJ is intended for percutaneous endoscopic placement to provide enteral nutrition and/or medication to patients requiring nutritional support, and gastric decompression. This device is indicated for adult use only.

Source page: https://510kreport.com/device/K183336
Methodology: https://510kreport.com/methodology