# K072348: Precision Oxygen Concentrator

- Pathway: 510(k) (Abbreviated)
- Applicant: Precision Medical, Inc.
- Decided: Oct 27, 2008 after 433 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: 2 generations back to K972614 (1998). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061261: L4 Oxygen Concentrator, Respironics, Inc. (2006) Summary page 1.

## Indications for use
The Precision Medical Concentrator is intended to provide supplemental oxygen to persons requiring oxygen therapy. The device is not intended to be life supporting or life sustaining. The concentrator is intended for use in the home or hospital institutional environment.

Source page: https://510kreport.com/device/K072348
Methodology: https://510kreport.com/methodology