# K131386: EZ-OX Plus Generation II

- Pathway: 510(k) (Traditional)
- Applicant: Air Liquide Healthcare America
- Decided: Mar 14, 2014 after 304 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 2.

## Most influential descendants
- K142149: Oxytote Infinity Series Vipr Systems (2015), 0 descendants of its own

## Indications for use
The EZ-OX Plus Generation Illis an integrated portable oxygen delivery system intended to provide supplemental oxygen to patients. When administered by propeuly trained personnel for oxygen deficiency and resuscitation, the EZ-OX Plus Generation IllIs for emergency use only. For all other medical applications, the device Is Rx only.

Source page: https://510kreport.com/device/K131386
Methodology: https://510kreport.com/methodology