Accurkardia, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2025-12-22
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K252361 | AccurECG Analysis System (v2.0) | DPS | 2025-12-22 | View |
| 510(k) | K223013 | AccurECG Analysis System | DPS | 2023-06-23 | View |
No matching devices.