# K990389: Moss Gastrostomy Tube

- Pathway: 510(k) (Traditional)
- Applicant: Moss Tubes, Inc.
- Decided: Mar 22, 1999 after 42 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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.

## Most influential descendants
- K190414: Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV (2019), 0 descendants of its own

## Indications for use
Used for gastric and proximal duodenal decompression plus duodenal feeding.

Source page: https://510kreport.com/device/K990389
Methodology: https://510kreport.com/methodology