# K092918: Pari Vios

- Pathway: 510(k) (Traditional)
- Applicant: Pari Respiratory Equipment, Inc.
- Decided: Feb 4, 2010 after 135 days
- Product code: CAF (Nebulizer (Direct Patient Interface))
- Device class: 2
- Regulation: 21 CFR 868.5630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K963924 (1996). 4 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061381: LC Star with Nasal Adapter, Pari Innovative Manufacturers, Inc. (2006) Summary page 1.
- K002862: Proneb Ultra Model Number 85B0100, Pari Holding Co. (2001) Summary page 1.

## Most influential descendants
- K191270: Proneb Max (2020), 0 descendants of its own
- K131881: Ombra Table Top Compressor (2013), 0 descendants of its own

## Indications for use
The PARI Vios is a tabletop, AC-powered air compressor intended to provide a source of compressed air for use with jet nebulizers. The PARI Vios is intended for adult and pediatric patients for use in hospital, clinic, or home environments.

Source page: https://510kreport.com/device/K092918
Methodology: https://510kreport.com/methodology