# K935370: Miniox IA Oxygen Analyzer

- Pathway: 510(k) (Traditional)
- Applicant: Minesafety Appliances Co.
- Decided: Aug 2, 1994 after 271 days
- Product code: CAW (Generator, Oxygen, Portable)
- Device class: 2
- Regulation: 21 CFR 868.5440
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
29 later devices descend from it; 1 cites it directly.
3 of 30 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
- K973282: Handi Oxygen Analyzer (1998), 28 descendants of its own
- K051857: Veo Multigas Monitor for Pocket PC, Model 400221 (2005), 16 descendants of its own
- K081601: Veo Multigas Monitor for Pocket PC (2008), 12 descendants of its own
- K123043: Irma C02 Model 200101; Irma AX 200601 (2012), 11 descendants of its own
- K023565: Oxicheck (2003), 10 descendants of its own

Source page: https://510kreport.com/device/K935370
Methodology: https://510kreport.com/methodology