FDA 510(k) Applications Submitted by Heuron Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K203142 | 10/20/2020 | Veuron-Brain-pAb | Heuron Co., Ltd. |
| K203279 | 11/06/2020 | Veuron-Brain-mN1 | Heuron Co., Ltd. |
| K213801 | 12/06/2021 | Veuron-Brain-pAb2 | Heuron Co., Ltd. |
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