FDA 510(k) Applications Submitted by Diality, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K243607 | 11/21/2024 | Moda-flx Hemodialysis SystemÖ Cartridge (102121-001 ) | Diality, Inc. |
| K233798 | 11/29/2023 | Moda-flx Hemodialysis System and Cartridge | Diality, Inc. |
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