FDA 510(k) Applications Submitted by VSI Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K221286 | 05/03/2022 | CLAROX | VSI Co., Ltd. |
| K221417 | 05/16/2022 | CLAROX plus (Model: VX-100) | VSI Co., Ltd. |
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