# K190414: Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV

- Pathway: 510(k) (Special)
- Applicant: Moss Tubes, Inc.
- Decided: Jun 14, 2019 after 113 days
- Product code: PIF (Gastrointestinal Tubes With Enteral Specific Connectors)
- 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
Longest line of descent: 1 generation back to K984629 (1999). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K990389: Moss Gastrostomy Tube, Moss Tubes, Inc. (1999) Summary page 6.
- K984629: Moss Tubes, Inc. Nasal Tube - Mark IV, Moss Tubes, Inc. (1999) Summary page 6.

## Indications for use
The Moss Gastrostomy Tube is used for gastric and proximal duodenal decompression plus duodenal feeding in adult populations. The Moss Nasal Tube is used for decompression and simultaneous feeding in adult populations.

Source page: https://510kreport.com/device/K190414
Methodology: https://510kreport.com/methodology