# K202539: Nutriglide (TM) Nasal Feeding Tube

- Pathway: 510(k) (Traditional)
- Applicant: Applied Medical Technology, Inc.
- Decided: Oct 29, 2020 after 57 days
- Product code: KNT (Tubes, Gastrointestinal (And Accessories))
- Device class: 2
- Regulation: 21 CFR 876.5980
- Recalls of this device: 6 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K821906 (1982). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K821906: Corpak Enteric Feeding Tube W/Guide Tip, Corpak Medsystems (1982) Summary page 4.
- K831328: Neonatal Nasogastric Feeding Tube-, Corpak Medsystems (1983) Summary page 4.

## Most influential descendants
- K241169: Entarik NI Feeding Tube System (2024), 0 descendants of its own

## Recalls of this device
- Oct 6, 2025 · Class II · Z-0498-2026: The nasal feeding tube may be occluded
- Oct 6, 2025 · Class II · Z-0496-2026: The nasal feeding tube may be occluded
- Oct 6, 2025 · Class II · Z-0497-2026: The nasal feeding tube may be occluded
- Oct 6, 2025 · Class II · Z-0494-2026: The nasal feeding tube may be occluded
- Oct 6, 2025 · Class II · Z-0495-2026: The nasal feeding tube may be occluded
- Aug 12, 2025 · Class II · Z-0127-2026: The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.

## Indications for use
The NutriGlide™ Nasal Feeding Tube is indicated for the administration of nutrition, fluids, and medications in neonatal, pediatric, and adult patients.

Source page: https://510kreport.com/device/K202539
Methodology: https://510kreport.com/methodology