# K950867: Medi - Pump

- Pathway: 510(k) (Traditional)
- Applicant: Thomas Industries
- Decided: Apr 19, 1995 after 51 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; 1 cites 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
- K991685: Halolite Aad System with Dedicated Compressor (1999), 11 descendants of its own
- K030747: Prodose Aad System (2004), 10 descendants of its own
- K042991: I-Neb Aad System (2005), 6 descendants of its own
- K100380: Altera Nebulizer System, Model 678G1002 (2010), 4 descendants of its own
- K112859: Erapid Nebulizer System (2012), 3 descendants of its own

Source page: https://510kreport.com/device/K950867
Methodology: https://510kreport.com/methodology