Vas-Cath, Inc. - FDA 510(k) Cleared Devices
Recent clearances: OPTI-PLAST (CENTURION) 5.5F ANGIOPLASTY CATHETER, NIAGARA DUAL LUMEN CATHETER, ULTRAVERSE PTA CATHETER
27
Total
27
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vas-Cath, Inc. General Hospital ✕
2 devices