| Device Type ID | 2244 |
| Device Name | Fibrinogen And Split Products, Antigen, Antiserum, Control |
| Regulation Description | Fibrinogen Determination System. |
| Regulation Medical Specialty | Hematology |
| Review Panel | Hematology |
| Premarket Review | Office Of In Vitro Diagnostics And Radiological Health (OIR)
|
| Submission Type | 510(k) |
| CFR Regulation Number | 864.7340 [🔎] |
| FDA Device Classification | Class 2 Medical Device |
| Product Code | DAZ |
| GMP Exempt | No |
| Summary MR | Ineligible |
| Implanted Device | No |
| Life Support Device | No |
| Third Party Review | Not Third Party Eligible |