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

FDA 510(k) Number Submission Date Device Name Applicant
K200860 04/01/2020 HANAROSTENT Esophagus TTS (CCC), HANAROSTENT Esophagus TTS (NCN) M.I. Tech Co., Ltd
K201160 04/30/2020 HANAROSTENT Esophagus (CCC), HANAROSTENT Esophagus (NCN) M.I. Tech Co., Ltd


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