# K063096: Precision Oxygen Monitor

- Pathway: 510(k) (Abbreviated)
- Applicant: Precision Medical, Inc.
- Decided: Feb 27, 2007 after 140 days
- Product code: CCL (Analyzer, Gas, Oxygen, Gaseous-Phase)
- Device class: 2
- Regulation: 21 CFR 868.1720
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K911344 (1991). 1 ancestor in all.
5 later devices descend from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K911344: Cerion Hand Held Oxygen Analyzer, Ceramatec, Inc. (1991) Summary page 1.

## Most influential descendants
- K153659: MaxO2ME (2016), 4 descendants of its own
- K221734: Maxtec MaxO2 ME+p (2023), 2 descendants of its own
- K251245: OxyMinder Pro (10310) (2025), 0 descendants of its own
- K231895: Maxtec MaxBlend2+p (2023), 0 descendants of its own
- K213948: OxyMinder (2022), 0 descendants of its own

## Indications for use
The Precision Medical Oxygen Monitor is intended to measure the concentration of oxygen being delivered to the patient. The oxygen monitor is not intended as a life supporting device.

Source page: https://510kreport.com/device/K063096
Methodology: https://510kreport.com/methodology