Illumina, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
Advertisement
Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K124006 | ILLUMINA MISEQDX CYSTIC FIBROSIS 139-VARIANT ASSAY | PFR | 2013-11-19 | View |
| 510(k) | K132750 | ILLUMINA MISEQDX CYSTIC FIBROSIS CLINICAL SEQUENCING ASSAY | PFS | 2013-11-19 | View |
| 510(k) | K093128 | ILLUMINA BEADXPRESS SYSTEM | NSU | 2010-04-28 | View |
| 510(k) | K093129 | ILLUMINA VERNCODE GENOTYPING TEST FOR FACOR V AND FACTOR II | NPQ | 2010-04-28 | View |
No matching devices.
Advertisement