FDA 510(k) Applications Submitted by Fanny Patoureaux
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K223902 | 12/28/2022 | FibroScan« device (Models: 502 Touch, 530 Compact, 430 Mini+, 230, and 630) | Echosens |
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