# K981629: Nutrisafe Enteral Feeding Tube

- Pathway: 510(k) (Traditional)
- Applicant: Schiff & Co.
- Decided: Feb 4, 1999 after 273 days
- Product code: FPD (Tube, Feeding)
- 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Indications for use
For nasogastric/oralgastric enteral feeding, incorporating safety connectors which eliminate the risk of accidental connection of an L.V. system to the enteral system, or the enteral system to an L.V. system.

Source page: https://510kreport.com/device/K981629
Methodology: https://510kreport.com/methodology