FDA 510(k) Applications Submitted by MANAMED, INC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160318 | 02/05/2016 | PlasmaFlow | MANAMED, INC |
| K200353 | 02/13/2020 | ManaFlow | ManaMed, Inc |
| K231569 | 05/31/2023 | ManaFlexx 2 (model: MF002-RX, MF002-OTC) | ManaMed, Inc |
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