Bipore, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER, BIPORE BALLOON DILATION CATHETER, BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER
10
Total
10
Cleared
0
Denied
FDA 510(k) Regulatory Record - Bipore, Inc. Gastroenterology & Urology ✕
1 devices