FDA 510(k) Applications Submitted by Mark Qian
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K192957 | 10/21/2019 | VivaChek Blood Glucose and B-Ketone Monitoring System | Vivachek Biotech (Hangzhou) Co., Ltd |
| K223722 | 12/12/2022 | MIO Blood Glucose Monitoring System | Mio Labs Inc. |
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