AliveCor, Inc.
FDA 510(k) & PMA Approved Devices — 13 products
Total Devices13
Categories4
Latest FDA decision2026-01-09
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K252589 | Corvair Monza | MHX | 2026-01-09 | View |
| 510(k) | K231010 | Corvair | MHX | 2024-06-07 | View |
| 510(k) | K232035 | Impala | DPS | 2024-06-07 | View |
| 510(k) | K220350 | KardiaMobile 6L | DXH | 2022-05-25 | View |
| 510(k) | K212662 | AliveCor QT Service | DQK | 2022-04-26 | View |
| 510(k) | K211668 | KardiaMobile Card | DXH | 2021-11-30 | View |
| 510(k) | K210753 | KardiaMobile 6L | DXH | 2021-06-30 | View |
| 510(k) | K201985 | KardiaAI | DQK | 2020-11-12 | View |
| 510(k) | K191406 | KardiaMobile, KardiaStation | DXH | 2020-01-24 | View |
| 510(k) | K183319 | Triangle System | DXH | 2019-05-10 | View |
| 510(k) | K182396 | KardiaMobile, KardiaStation | DXH | 2019-04-12 | View |
| 510(k) | K181823 | KardiaAI | DQK | 2019-03-11 | View |
| 510(k) | K171816 | Kardia Band System | DXH | 2017-11-16 | View |
No matching devices.