Caredx, Inc.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest FDA decision2023-09-13
SEC Filings: 1 filings on record. Latest: 10-Q (2026-07-30). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K221640 | AlloMap Heart Molecular Expression Testing | OJQ | 2023-09-13 | View |
No matching devices.