# K984310: Moss Tubes, Inc, All Silicone Gastrostomy Tube

- Pathway: 510(k) (Traditional)
- Applicant: Moss Tubes, Inc.
- Decided: Feb 24, 1999 after 84 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
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
Used to feed nutrients directly into the stomach through a stoma in the abdomen. The tubes are intended as a replacement device and are labeled as such.

Source page: https://510kreport.com/device/K984310
Methodology: https://510kreport.com/methodology