# K971906: Jejenostomy Feeding Tube

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific Corp
- Decided: Aug 20, 1997 after 89 days
- Product code: FPD (Tube, Feeding)
- 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.
5 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Bard’s Jejunal Feeding/Gastric Decompression Tube: named in the summary without a submission number
- (no number) Corpak’s Corflo-Ultra Jejunostomy Tube: named in the summary without a submission number

## Most influential descendants
- K072476: Through-the-Peg (TTP) Jejunostomy Tube Kit (2007), 4 descendants of its own
- K081739: 2-Port Through-the-Peg (TTP) Jejunostomy Tube Kit (2008), 2 descendants of its own
- K133096: Abb Vie J (2014), 1 descendant of its own
- K142816: AbbVie J (2015), 0 descendants of its own
- K091340: Through the -Peg (TTP) Jejunal Feeding Tube Kit, Model M00566320,M00566330, M00566340, M00566350 (2009), 0 descendants of its own

## Indications for use
The TTP J-Tube is indicated for enteral nutritional support and decompression where feeding via the upper gastrointestinal tract is contraindicated. This includes, post upper G.1. tract surgery, radiation therapy, chemotherapy, reflux and other conditions associated with nausea, vomiting and possible aspiration.

Source page: https://510kreport.com/device/K971906
Methodology: https://510kreport.com/methodology