# K173808: Voutia™

- Pathway: 510(k) (Traditional)
- Applicant: Jeffrey Ward Cash, Dds
- Decided: Jul 27, 2018 after 224 days
- Product code: LFD (Saliva, Artificial)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K874106 (1988). 11 ancestors in all.
No later device cites it as a predicate yet.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110116: Xeros Dry Mouth Pump, Lorin Technologies Corporation (2011) Summary page 4.

## Indications for use
The Voutia™ system is indicated to provide relief of dry mouth by coating, moistening, and lubricating oral structures thereby relieving the symptoms of xerostomia (dry mouth).

Source page: https://510kreport.com/device/K173808
Methodology: https://510kreport.com/methodology