FDA 510(k) Applications for Medical Device Product Code "QEJ"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K240925 | Marizyme | DuraGraft Vascular Conduit Solution | 05/01/2024 |
| DEN230002 | Marizyme, Inc. | DuraGraft | 10/04/2023 |
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