| Device Type ID | 4893 |
| Device Name | Immunohistochemistry Assay, Antibody, Progesterone Receptor |
| Regulation Description | Immunohistochemistry Reagents And Kits. |
| Regulation Medical Specialty | Hematology |
| Review Panel | Pathology |
| Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR)
|
| Submission Type | 510(k) |
| CFR Regulation Number | 864.1860 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | MXZ |
| GMP Exempt | No |
| Summary MR | Eligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Eligible For Accredited Persons Program |