Asahi Intecc Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SAYA 86 Radial Access Guide Catheter, CHIKAI Nexus petit, Branchor X Balloon Guide Catheter
84
Total
84
Cleared
0
Denied
FDA 510(k) Regulatory Record - Asahi Intecc Co., Ltd. Gastroenterology & Urology ✕
1 devices