# K083210: Corflo Anti IV Enteral Feeding Tube

- Pathway: 510(k) (Traditional)
- Applicant: Corpak Medsystems
- Decided: Dec 29, 2008 after 59 days
- Product code: FPD (Tube, Feeding)
- Device class: 2
- Regulation: 21 CFR 876.5980
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
19 later devices descend from it; 3 cite it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K140581: Cedic Enteral Distal End Enfit Transition Connector, Cedic Enteral Enfit Transition Connector for Medication Port (2014), 8 descendants of its own
- K112511: Dobbhoff Dual Port Feeding Tube (2012), 8 descendants of its own
- K123555: Kangaroo Feeding Tubes with Iris Technology (2014), 4 descendants of its own
- K142327: smARTrack Feeding Tube System (2015), 2 descendants of its own
- K230206: Entarik Feeding Tube System; Entarik Feeding Tube (2023), 1 descendant of its own

## Recalls of this device
- Dec 13, 2017 · Class II · Z-1277-2018: The transmitting stylet within CORTRAK* 2 nasogastric/Nasointestinal (NG/NI) Feeding Tubes with ANTI-IV* connector (Product Code 20-9551Trak2A) may be visible within the window of the exit port of the

## Indications for use
The CORFLO® ANTI IV Enteral Feeding tube is intended for use in those patients who require intermittent or continuous tube feedings via the nasogastric or nasoenteric route.

Source page: https://510kreport.com/device/K083210
Methodology: https://510kreport.com/methodology