# K080082: Oxlife Independence Oxygen Concentrators

- Pathway: 510(k) (Traditional)
- Applicant: Oxlife, LLC
- Decided: Apr 16, 2008 after 96 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
Longest line of descent: 4 generations back to K933081 (1994). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K013931: Omni Oxygen System, Model 1000, Sequal Technologies, Inc. (2002) Summary page 1.

## Indications for use
The OxLife Oxygen Concentrators are indicated for the administration for supplemental oxygen.

Source page: https://510kreport.com/device/K080082
Methodology: https://510kreport.com/methodology