# K072756: Non-IV Adapter for Infant NG Tube

- Pathway: 510(k) (Traditional)
- Applicant: Promedic, Inc.
- Decided: Dec 19, 2007 after 83 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: 4 generations back to K810156 (1981). 6 ancestors in all.
5 later devices descend from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052903: Pediatric Feeding Tube, Promedic, Inc. (2005) Summary page 1.

## Most influential descendants
- K082710: Safechild Enteral Feeding Tube and Accessories and Feeding Tube Extension Set (2009), 4 descendants of its own
- K092628: Enteral Feeding Tube and Accessories, Feeding Tube Extension Set (2010), 2 descendants of its own
- K162340: Stomach Tube (2017), 0 descendants of its own
- K112863: Enteral Administration Set with Solution Container, Enteral Administration Set, Enteral Extension Set with Minitube Conn (2012), 0 descendants of its own
- K100700: Med-RX Pediatric Feeding Tubes and Accessories (2010), 0 descendants of its own

## Indications for use
A non-IV connector for use with Infant Feeding tubes that are intended to be placed into the stomach to permit the introduction of fluids as directed by the physician. Intended for nasogastric or orogastric placement. Limited to < 30 day placement. Not intended for transpyloric placement.

Source page: https://510kreport.com/device/K072756
Methodology: https://510kreport.com/methodology