# K120272: Ameritus Medical Enteral Feeding Extension Set

- Pathway: 510(k) (Traditional)
- Applicant: Kentec Medical, Inc.
- Decided: Feb 17, 2012 after 18 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 K801558 (1980). 10 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K100288: Neomed Enteral Only Extension Set, Neomed, Inc. (2010) Summary page 1.
- K083786: Corflo Anti-IV Enteral Feeding Extension Set, Models 20-1006AIV-LB and 20-1030AIV-LB, Corpak Medsystems (2009) Summary page 1.
- K083791: Corflo Anti IV Enteral Feeding Set, Model: 20-1060AIV-S, Corpak Medsystems (2009) Summary page 1.

## Most influential descendants
- K180236: VR Medical Feeding Tube and Enteral Feeding Extension Set (EFES) (2019), 1 descendant of its own
- K200082: BD Univia RightFit Enteral Extension Sets and Transitional Adapters (2020), 0 descendants of its own

## Indications for use
The Ameritus® Enteral Feeding Extension Set is intended for use as an extension set for nasogastric/oralgastric or gastric tube enteral feeding tubes, incorporating safety connectors which help mitigate the risk of accidental misconnection with an I.V. system to the enteral system or the enteral system to an I.V. system. The Enteral Feeding Extension Set is indicated for use in neonatal and pediatnic patients in connection with an enteral feeding tube to provide nutrition via nasal or oral gastric placements. The Enteral Feeding Extension Set is a sterile disposable for single patient use only.

Source page: https://510kreport.com/device/K120272
Methodology: https://510kreport.com/methodology