# K935540: Pari-Master Modification

- Pathway: 510(k) (Traditional)
- Applicant: Pari Holding Co.
- Decided: Mar 17, 1995 after 486 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
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K062689: Sidestream Plus (2007), 0 descendants of its own
- K053203: Myneb Nebulizer, Model RDD100 (2005), 0 descendants of its own

Source page: https://510kreport.com/device/K935540
Methodology: https://510kreport.com/methodology