Arrow International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: AC3 IABP, AC3 Optimus IABP, AutoCAT2 Wave IABP, AutoCAT2 IABP, Arrow FiberOptix Intra-Aortic Balloon Catheter Kit, UltraFlex IAB
19
Total
17
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arrow International, Inc. Gastroenterology & Urology ✕
4 devices