Kaycor Intl., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: PANOURA ULTRA PAN AND PANOURA ULTRA PAN/CEPH PANORAMIC/CEPHALOMETRIC X-RAY UNIT
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Kaycor Intl., Ltd. Radiology ✕
3 devices