Terumo Cardiovascular Systems Corporation - FDA 510(k) Cleared Devices
Recent clearances: CDI OneView Monitoring System, Terumo Advanced Perfusion System 1, Capiox iCP Centrifugal Pump
29
Total
29
Cleared
0
Denied
FDA 510(k) Regulatory Record - Terumo Cardiovascular Systems Corporation General & Plastic Surgery ✕
2 devices