Xandar Kardian, Inc. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Xandar Kardian, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Vital Sign Monitoring Sensor (Model :XK300)
1
Total
1
Cleared
0
Denied
Xandar Kardian, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Last cleared in 2021. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Xandar Kardian, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Alira Health as regulatory consultant.
FDA 510(k) Regulatory Record - Xandar Kardian, Inc.
1 devices