# K133087: Abbvie Peg

- Pathway: 510(k) (Traditional)
- Applicant: AbbVie, Inc.
- Decided: Jun 19, 2014 after 262 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: 2 generations back to K014297 (2002). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030855: Modification to Endovive Initial Placement Peg Kit, Direct Pej Kit, Peg Safety Kit, Boston Scientific Corp (2003) Summary page 1.

## Most influential descendants
- K142793: AbbVie PEG (2015), 0 descendants of its own

## Indications for use
The AbbVie PEG is intended to provide long-term enteral access for administration of medication to the small intestine when used in conjunction with the AbbVie J, intestinal tube. As needed, enteral nutrition may be administered directly to the stomach in parallel with medication delivery to the intestine.

Source page: https://510kreport.com/device/K133087
Methodology: https://510kreport.com/methodology