Kaneka Pharma America, LLC - FDA 510(k) Cleared Devices
Recent clearances: i-ED COIL, Lacriflow CL, XPRESSWAY RX CATHETER (6F LD-VERISON)
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Kaneka Pharma America, LLC Neurology ✕
1 devices