FDA 510(k) Applications Submitted by M.I.Tech Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K190141 | 01/29/2019 | HANAROSTENT LowAx Colon/Rectum (NNN) | M.I.Tech Co., Ltd. |
| K202973 | 09/30/2020 | HANAROSTENT Benefit Biliary (NNN) | M.I.Tech Co., Ltd. |
| K183396 | 12/07/2018 | HANAROSTENT FASTTM Biliary (NNN) | M.I.Tech Co., Ltd. |
| K213251 | 09/30/2021 | HANAROSTENT Esophagus Asymmetric (CCC) | M.I.Tech Co., Ltd. |
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