Agilent Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
Total Devices7
Categories6
Latest Approval2025-08-15
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| PMA | P250004 | Immunohistochemistry test, DNA mismatch repair (MMR) Protein assay | QNH | 2025-08-15 | View |
| PMA | P230016 | Immunohistochemistry Assay, Antibody, Melanoma-associated antigen A4 | SBL | 2024-08-01 | View |
| PMA | P210026 | Immunohistochemistry assay, antibody, Ki-67 | QQT | 2021-10-12 | View |
| 510(k) | K163367 | GenetiSure Dx Postnatal Assay | PFX | 2017-08-11 | View |
| PMA | P030044 | Immunohistochemistry assay, antibody, epidermal growth factor receptor | NQF | 2017-05-16 | View |
| PMA | P150025 | Immunohistochemistry assay, antibody, programmed death-ligand 1 | PLS | 2016-12-01 | View |
| PMA | P150013 | Immunohistochemistry assay, antibody, programmed death-ligand 1 | PLS | 2016-12-01 | View |
No matching devices.