FDA 510(k) Applications for Medical Device Product Code "QFQ"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K240544 | Epitomee Medical Ltd. | Epitomee | 09/13/2024 |
| K230133 | Gelesis Inc. | Plenity | 01/19/2024 |
| DEN180060 | Gelesis, Inc. | Plenity | 04/12/2019 |
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