Arrow International, LLC - FDA 510(k) Cleared Devices
Recent clearances: AC3™ Range™ Intra-Aortic Balloon Pump, AC3™ Series IABP, Arrow 0.2 Micron Flat Filter, GVS
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Arrow International, LLC Anesthesiology ✕
1 devices