# K143060: Intelli-Ox

- Pathway: 510(k) (Traditional)
- Applicant: Air Liquide Healthcare
- Decided: May 21, 2015 after 209 days
- Product code: ECX (Cylinder, Compressed Gas, And Valve)
- Device class: 1
- Regulation: 21 CFR 868.2700
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K033897 (2004). 2 ancestors in all.
1 later device descends 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)
- K053117: EZ-OX Plus, Air Liquide Healthcare America (2006) Summary page 5.

## Most influential descendants
- K161179: Intelli-Ox (2017), 0 descendants of its own

## Indications for use
The Intelli-Ox is an integrated portable oxygen delivery system intended to provide supplemental oxygen to adults. When administered by properly trained personnel for oxygen deficiency and resuscitation, the Intelli-Ox is for emergency use only. For all other medical applications, the device is Rx only.

Source page: https://510kreport.com/device/K143060
Methodology: https://510kreport.com/methodology