# K914152: Sidestream Drug Nebulizer

- Pathway: 510(k) (Traditional)
- Applicant: Medic-Aid, Ltd.
- Decided: May 5, 1992 after 232 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.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K991725: Sidestream Nebulizer (1999), 2 descendants of its own
- K072163: Happyneb II, Happyneb Iii, Speedy, Nebby Plus and Myneb, Model 5 (2008), 0 descendants of its own
- K062484: Flaem Nuova RF6 Basic and RF6 Plus Nebulizers (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K914152
Methodology: https://510kreport.com/methodology