# K885339: Flow Thru 16,18,20,22 FR Replace. Gastro Tube Kit

- Pathway: 510(k) (Traditional)
- Applicant: Superior Healthcare Group, Inc.
- Decided: Mar 1, 1989 after 63 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
No predicates in its family tree.
3 later devices descend from it; 2 cite 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)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K142075: BI-Funnel Gastrostomy Feeding Tube, Tri-Funnel Gastrostomy Feeding Tube (2015), 1 descendant of its own
- 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
- K981323: Compat Mini-G Replacement Gastrostomy Tube (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K885339
Methodology: https://510kreport.com/methodology