# K003344: Medical Depot Nebulizer, Model Power Neb 2

- Pathway: 510(k) (Traditional)
- Applicant: Medical Depot, Inc.
- Decided: Mar 15, 2001 after 141 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K063449: Deluxe Nebulizer (2007), 0 descendants of its own
- K012006: Medical Depot Power Neb 1 (2001), 0 descendants of its own

Source page: https://510kreport.com/device/K003344
Methodology: https://510kreport.com/methodology