GIO
- Product code
- GIO
- Device name
- Tube, Collection, Capillary Blood
- Device class
- Class 1
- 21 CFR
- 21 CFR 864.6150
- Medical specialty
- Hematology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 22 (all years; only the last 3 years are listed here)
Official FDA classification page: GIO
Classification and pathway per current FDA publications. Data from openFDA (CC0).