VITAL SIGN MONITORING
FDA 510(k) cleared
Class II medical device
ISO 13485:2016 Quality
34 Journal Publications
FDA 510(K) CLASS II CLEARANCE USING RADAR
100% PRIVACY PROTECTED
KARDIAN WORKS WITH YOU
SENSE THROUGH ALL TYPES OF FURNITURE AND CLOTHING
CMS issued key eligibility criteria for the use of CPT code 99454 within
the CY2021 Payment Policies under the Physician Fee Schedule, Final Rule:
Xandar Kardian XK300-H shown. CES 2022 Demo. Market Launch: Summer, 2022.
Device must perform physiologic monitoring of parameters such as weight, blood pressure, pulse oximetry for at least 16 over a 30-day period?
YES, XK300 monitors RHR + RR continuously & automatically every day.
The device is an FDA-approved medical device?
YES, XK300 is FDA 510(k) cleared.
Digitally/automatically uploads patient physiologic data?
YES, XK300 automatically uploads patient data securely in real-time via LTE.
Device must be used to collect and transmit reliable and valid physiologic data that allow understanding of a patient`s health status in order to develop and manage a plan of treatment?
• YES, XK300 collects and transmits RHR + RR data to clinicians to better manage their plan of treatment.
The XK300 can be installed in your facility to help prevent hospital readmissions and costly ER visits.
Long Term Care
Monitor your residents in memory care as a safety measure and long term for chronic conditions with the same sensor, XK300.
Find out more on what Xandar Kardian’s FDA 510(k) cleared radar technology can do for you. Behavioural health monitoring, substance control rehab facilities, correctional facilities, emergency field operations are just other application examples!