Innerdyne, Inc. - FDA 510(k) Cleared Devices
Recent clearances: INNERDYNE RADIALLY EXPANDING VASCULAR ACCESS SYSTEM (REVAS), INNERDYNE RADIALLY EXPANDING DILATION, RED DEVICE, INNERDYNE GENERIC RADIALLY EXPANDING DILATION, G-RED DEVICE
12
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - Innerdyne, Inc. Gastroenterology & Urology ✕
2 devices