Pulse Oximetry FAQ

This FAQ has been compiled by our team of experts. Please submit your questions at the bottom of this page!

Pulse Oximetry FAQ Common pulse ox myths

Do pulse oximeters require regular calibrations while in clinical use?

Most pulse oximeters do not need to be calibrated by the user before they will work properly. During device development, the microprocessors of pulse oximeters are calibrated using reference SaO2 measurement data that are compiled from healthy volunteers. Volunteers are typically exposed to different levels of inspired oxygen to yield SaO2 ranging from around 75 to 100%.

There are devices such as the Fluke ProSim 8 that are designed to check if select manufacturers’ oximeters are functioning, but are not designed to validate accuracy.

References: Lifebox Pulse Oximetry Learning Module

Keywords: calibration

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About Community Device Data Raw Data Protocols Publications FAQ

Healthy Human Performance Tests

To meet ISO standards (80601-2-61) or FDA guideline adherence for clinical use, pulse oximeter performance must be tested in healthy humans in a laboratory setting. Independent device testing for the Open Oximetry Project follows our protocol consistent with ISO and FDA. Only devices labeled as ‘verified’ or ‘disputed’ have been independently tested by the Open Oximetry Project.
All other devices listed show data from manufacturers or published literature and have not been confirmed by the Open Oximetry Team. Scoring criteria will be modified based on evolving data on this topic. See the table below for scoring criteria for this category:

No Data

1 (red)

>4%

2 (red)

<4%

AND/OR Data suggesting Arms for dark skin color of >4%

AND/OR Data suggesting Arms for PI<1 in dark or light skin color of >4%

3 (yellow)

<4%

AND/OR Data suggesting Arms for dark skin color of 3-4%

AND/OR Data suggesting Arms for PI<1 in dark or light skin color of 3-4%

4 (green)

<3%

AND No data for or against performance problems in darker skin colors

AND No data for or against performance problems in low perfusion

5 (green)

<3%

AND Extended testing beyond ISO/FDA recommendations Criteria TBD April 2023

* only independently tested devices by OpenOximetry (Hypoxia Lab and Clinimark) get labeled as ‘verified’