# K162110: CORGRIP NG/NI Tube Retention System

- Pathway: 510(k) (Traditional)
- Applicant: Corpak Medsystems, Inc. A Division of Haylard Health
- Decided: Sep 15, 2016 after 48 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: 1 generation back to K133599 (2014). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133599: Corgrip, Corpak Medsystems (2014) Summary page 4.

## Indications for use
The CORGRIP Nasogastric/Nasointestinal (NG/NI) Tube Retention System is indicated for use with enteral feeding tubes of 8 FR and greater and NG decompression, suction and drainage tubes up to 18 FR to prevent inadvertent removal or displacement of the tubes for adult patients.

Source page: https://510kreport.com/device/K162110
Methodology: https://510kreport.com/methodology