# K142075: BI-Funnel Gastrostomy Feeding Tube, Tri-Funnel Gastrostomy Feeding Tube

- Pathway: 510(k) (Traditional)
- Applicant: Xeridiem (Formerly Mri)
- Decided: Jan 8, 2015 after 161 days
- Product code: PIF (Gastrointestinal Tubes With Enteral Specific Connectors)
- 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 K885339 (1989). 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)
- K885339: Flow Thru 16,18,20,22 FR Replace. Gastro Tube Kit, Superior Healthcare Group, Inc. (1989) Summary page 4.

## Most influential descendants
- K171347: Bi-Funnel and Tri-Funnel Gastrostomy Feeding Tubes with ENFit Connection, Entuit Gastrostomy BR Balloon Retention Feeding Tube with ENFit Connection (2017), 0 descendants of its own

## Indications for use
The G-Tube is indicated for placement in adult populations that require enteral feeding, medication administration or gastric decompression through an established gastrointestinal stoma tract.

Source page: https://510kreport.com/device/K142075
Methodology: https://510kreport.com/methodology