Vantis Vascular, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CrossFAST Integrated Microcatheter Advanced Delivery System, CrossFAST™ Integrated Microcatheter Guide Extension System (CFM55)
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vantis Vascular, Inc. Cardiovascular ✕
2 devices