Illumina, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2026-08-14
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| PMA | P230011 | Next generation sequencing oncology panel, somatic or germline variant detection system | PQP | 2026-08-14 | View |
| PMA | P160038 | Next generation sequencing oncology panel, somatic or germline variant detection system | PQP | 2023-02-17 | View |
No matching devices.