Accutech Medical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ACCUTECH FAMILY OF POWERFLEX LASER DELIVERY DEVICES, ACCUTECH ENDOLITE PROBE
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Accutech Medical Technologies, Inc. Gastroenterology & Urology ✕
1 devices