I'm quite confused by Delta's website
https://www.delta.com/us/en/accessib...ces-medication
Certain PAP devices are required to have a manufacturer label stating compliance with RTCA DO-160 Section 21 Cat H, meaning it can be used on board the aircraft. Please refer to the chart below for information about your device.
If you do not see your device listed, and it does not have the RTCA DO-160 Section 21 Cat H label, please contact our accessibility assistance line at 404-209-3434 for approval
My device (Philips DreamStation Auto) clearly is marked "M", not "H", and from what I can see, M is actually the one for passenger cabin use (
https://do160.org/emission-of-radio-frequency-energy/ ). Is Delta's page wrong, or can I just not understand what is being communicated?
thanks,
RDP