# K942444: 3002 Aeromax

- Pathway: 510(k) (Traditional)
- Applicant: Medical Industries America, Inc.
- Decided: Mar 10, 1995 after 291 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.
4 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K992285: Salter Aire Compressor (2000), 3 descendants of its own
- K082878: Nevoni Classic, Model 6600-PO (2008), 0 descendants of its own
- K072163: Happyneb II, Happyneb Iii, Speedy, Nebby Plus and Myneb, Model 5 (2008), 0 descendants of its own
- K062014: Families of Master Neb, Primo Neb, SC03, Neb Aid, 4.2.Neb, Q03, FJ03, and Walkie-Neb (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K942444
Methodology: https://510kreport.com/methodology