# K914836: Omron Compressor Nebulizer- Model NE-C09

- Pathway: 510(k) (Traditional)
- Applicant: Omron Healthcare, Inc.
- Decided: May 6, 1992 after 194 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.
12 later devices descend from it; 4 cite it directly.
0 of 13 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
- K060811: Omron Compressor Systems, Models NE-C28,NE-C30 (2006), 4 descendants of its own
- K110860: Comp a-I-R (2011), 3 descendants of its own
- K032170: Transneb Compressor W/Nebulizer, Model 5000 (2004), 3 descendants of its own
- K042483: Invacare Pro, Compact and Portable Desktop (2005), 2 descendants of its own
- K031413: Vigormist Compressor Nebulizer (2003), 1 descendant of its own

Source page: https://510kreport.com/device/K914836
Methodology: https://510kreport.com/methodology