FDA 510(k) Applications Submitted by Biomerieux Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K240279 | 02/01/2024 | VIDAS TBI (GFAP, UCH-L1) | Biomerieux Inc. |
| K234012 | 12/19/2023 | VITEK COMPACT PRO | bioMerieux Inc. |
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