# K821906: Corpak Enteric Feeding Tube W/Guide Tip

- Pathway: 510(k) (Traditional)
- Applicant: Corpak Medsystems
- Decided: Jul 13, 1982 after 15 days
- Product code: KNT (Tubes, Gastrointestinal (And Accessories))
- 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.
6 later devices descend from it; 3 cite it directly.
0 of 7 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
- K182915: ENvizion Medical ENvue; ENvizion Medical Enteral Feeding Tube (2019), 2 descendants of its own
- K202539: Nutriglide (TM) Nasal Feeding Tube (2020), 1 descendant of its own
- K191387: ENvizion Medical ENVue SYSTEM, ENvizion Medical Enteral Feeding Tube (2019), 1 descendant of its own
- K241169: Entarik NI Feeding Tube System (2024), 0 descendants of its own
- K202748: Enteral Feeding Catheter (2021), 0 descendants of its own

## Recalls of this device
- Jan 26, 2012 · Not classified · Z-1080-2012: The wrong size Twoomey adapter was packaged with the Jejunal tube.

Source page: https://510kreport.com/device/K821906
Methodology: https://510kreport.com/methodology