FDA 510(k) Applications Submitted by INDIBA S.A.U
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K241107 | 04/22/2024 | Indiba Diathermia Radiofrequency Deep Care Device (Deep care IDC0409/EVONY ); Indiba Diathermia Radiofrequency Activ Device (Activ ACT0309/CT9) | INDIBA S.A.U |
| K243139 | 09/30/2024 | Reverso Pro System | Indiba S.A.U |
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