Urotronic, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Optilume® High Pressure Urological Balloon Dilation Catheter, Optilume Basic Urological Balloon Dilation Catheter
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Urotronic, Inc. Gastroenterology & Urology ✕
2 devices