# K133129: Abbvie NJ

- 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: 1 generation back to K833621 (1983). 1 ancestor in all.
1 later device descends 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)
- K833621: Entri Flex Feeding Tube, Biosearch Medical Products, Inc. (1983) Summary page 1.

## Most influential descendants
- K142792: AbbVie NJ (2015), 0 descendants of its own

## Indications for use
The AbbVie NJ is intended to provide short-term enteral access for administration of medication to the small intestine.

Source page: https://510kreport.com/device/K133129
Methodology: https://510kreport.com/methodology