# K060399: LC Sprint Nebulizer

- Pathway: 510(k) (Traditional)
- Applicant: Pari Innovative Manufacturers, Inc.
- Decided: Mar 2, 2006 after 15 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: 1 generation back to K963924 (1996). 2 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023602: Small Volume Nebulizer, Allegiance Healthcare Corporation (2003) Summary page 1.
- K963924: LC Star Reusable Nebulizer 22F50 and LC Star Disposable Nebulizer 22F70, Pari Holding Co. (1996) Summary page 1.

## Most influential descendants
- K092560: Pari Sinus (2010), 0 descendants of its own
- K090730: Akita Jet (2009), 0 descendants of its own
- K062158: LC Sprint Star (2006), 0 descendants of its own

## Indications for use
The LC Sprint is a handheld nebulizer, designed to aerosolize medication approved for nebulization and prescribed by a physician. The LC Sprint is intended for adult and pediatric patients consistent with the indications for the aerosol medication.

Source page: https://510kreport.com/device/K060399
Methodology: https://510kreport.com/methodology