FDA 510(k) Applications for Medical Device Product Code "QTD"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K232544 | Apollo Endosurgery Inc. | Apollo ESG NXT System, Apollo REVISE NXT System | 09/18/2023 |
| DEN210045 | Apollo Endosurgery, Inc. | APOLLO ESG System, APOLLO ESG SX System, APOLLO REVISE System, APOLLO REVISE SX System | 07/12/2022 |
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