Xr, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Xr, LLC has 1 FDA 510(k) cleared medical devices. Based in Huntington Beach, US.
Last cleared in 2021. Active since 2021. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Xr, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Med-Device Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Xr, LLC
1 devices