FDA 510(k) Applications Submitted by Chungwoo Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K222709 | 09/08/2022 | Retraction, CWM-910T, APOLEX Tite | Chungwoo CO., LTD. |
| K233120 | 09/27/2023 | CWM-930S, FIXER DV9 | Chungwoo Co., Ltd. |
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