M.I. Tech Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: HANAROSTENT Esophagus Upper (CCC), HANAROSTENT Esophagus Asymmetric (CCC), HANAROSTENT Esophagus (CCC), HANAROSTENT Esophagus (NCN)
14
Total
11
Cleared
0
Denied
FDA 510(k) Regulatory Record - M.I. Tech Co., Ltd. Neurology ✕
1 devices