CorDx, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2026-06-01
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K253882 | CorDx Tyfast COVID-19 Ag Rapid Test Rx | QVF | 2026-06-01 | View |
| 510(k) | K240728 | CorDx Tyfast COVID-19 Ag Rapid Test; CorDx COVID-19 Ag Test | QYT | 2024-06-21 | View |
No matching devices.