FDA 510(k) Applications Submitted by AIOBIO Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K221275 | 05/02/2022 | Qraycam PRO | Aiobio Co., Ltd. |
| K183121 | 11/09/2018 | Qraypen | AIOBIO Co., Ltd. |
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