Maquet Cardiopulmonary, AG - FDA 510(k) Cleared Devices
Recent clearances: QUADROX-i Adult/Small Adult Oxygenators, ANTEGRADE CARDIOPLEGIA CANNULA(N-TYPE), NEONATAL VENOUS HARDSHELL CARDIOTOMY RESERVIOR, PEDIATRIC VENOUS HARDSHELL CARDIOTOMY RESERVIOR, NEONATAL VENOUS HARDHSH
44
Total
44
Cleared
0
Denied
FDA 510(k) Regulatory Record - Maquet Cardiopulmonary, AG Gastroenterology & Urology ✕
1 devices