Vivio® LVEDP System is an AI-enabled medical device from Avicena, LLC, listed by FDA (510(k), K223905) with a decision date of 2023-10-06. Review panel: Cardiovascular.
| FDA submission number | K223905 |
|---|---|
| Pathway | 510(k) |
| Company | Avicena, LLC |
| Review panel (specialty) | Cardiovascular |
| FDA decision date | 2023-10-06 |
| Decision | Substantially Equivalent |
| Product code | QUO |
| Classification | Adjunctive Heart Failure Status Indicator |
| Device class | 2 |
| Regulation number | 870.2200 |
| Review time (calendar days) | 282 |
| Applicant country | US |
Official FDA database record · FDA AI-enabled device list
All Cardiovascular AI devices · Full device index
Data from FDA's AI-enabled device list and openFDA. Informational only; verify against the FDA record.