Venocare, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Ruby Intravascular Catheter, Navi™ Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG), Ruby Intravascular Catheter
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Venocare, Inc. General Hospital ✕
3 devices