GKT
- Product code
- GKT
- Device name
- Separator, Automated, Blood Cell, Diagnostic
- Device class
- Class 2
- 21 CFR
- 21 CFR 864.9245
- Medical specialty
- Hematology
- Marketing pathway
- 510(K)
- 510(k) clearances (all years, FDA)
- 10 (all years; only the last 3 years are listed here)
Official FDA classification page: GKT
Classification and pathway per current FDA publications. Data from openFDA (CC0).