FDA 510(k) Applications Submitted by Shenzhen YHLO Biotech Co., LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K223690 | 12/09/2022 | iFlash-HCG; Chemiluminescence Immunoassay Analyzer (Model: iFlash 3000-C) | Shenzhen YHLO Biotech Co., LTD. |
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