M.I.Tech Co., Ltd.
FDA 510(k) medical device clearances.
Top product codes for M.I.Tech Co., Ltd.
Recent clearances by M.I.Tech Co., Ltd.
- K253327 — HANAROSTENT Esophagus Upper (CCC)
- K213251 — HANAROSTENT Esophagus Asymmetric (CCC)
- K201160 — HANAROSTENT Esophagus (CCC), HANAROSTENT Esophagus (NCN)
- K202973 — HANAROSTENT Benefit Biliary (NNN)
- K201342 — HANAROSTENT Trachea/Bronchium (CCC)
- K200860 — HANAROSTENT Esophagus TTS (CCC), HANAROSTENT Esophagus TTS (NCN)
- K190141 — HANAROSTENT LowAx Colon/Rectum (NNN)
- K183396 — HANAROSTENT FASTTM Biliary (NNN)
- K183616 — HANAROSTENT LowAx Colon/Rectum (NNN), HANAROSTENT LowAx Duodenum/Pylorus (NNN)
- K180180 — HANAROSTENT LowAxTM Colon/Rectum (NNN), HANAROSTENT LowAxTM Duodenum/Pylorus (NNN)
- K160893 — HANAROCare ReJu
- K111149 — HANAROSTENT BILIARY (NNN)
- K093537 — HANAROSTENT ESOPHAGUS (CCC)
- K072094 — CHOOSTENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.