HHT
- Product code
- HHT
- Device name
- Spatula, Cervical, Cytological
- Device class
- Class 2
- 21 CFR
- 21 CFR 884.4530
- Medical specialty
- Obstetrics/Gynecology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 73
Official FDA classification page: HHT
Classification and pathway per current FDA publications. Data from openFDA (CC0).