FDA 510(k) Applications Submitted by M.I. Tech Co., Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K093537 11/16/2009 HANAROSTENT ESOPHAGUS (CCC) M.I. TECH CO., LTD.
K072094 07/30/2007 CHOOSTENT M.I. TECH CO., LTD.
K180180 01/23/2018 HANAROSTENT LowAxTM Colon/Rectum (NNN), HANAROSTENT LowAxTM Duodenum/Pylorus (NNN) M.I. Tech Co., Ltd.
K201342 05/20/2020 HANAROSTENT Trachea/Bronchium (CCC) M.I. Tech Co., Ltd.
K183616 12/26/2018 HANAROSTENT LowAx Colon/Rectum (NNN), HANAROSTENT LowAx Duodenum/Pylorus (NNN) M.I. Tech Co., Ltd.
K111149 04/25/2011 HANAROSTENT BILIARY (NNN) M.I. TECH CO., LTD.


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