GFX
- Product code
- GFX
- Device name
- Fibrinogen Standard
- Device class
- Class 2
- 21 CFR
- 21 CFR 864.7340
- Medical specialty
- Hematology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 3
Official FDA classification page: GFX
Classification and pathway per current FDA publications. Data from openFDA (CC0).