HGF
- Product code
- HGF
- Device name
- Source, Abortion Unit, Vacuum
- Device class
- Class 2
- 21 CFR
- 21 CFR 884.5070
- Medical specialty
- Obstetrics/Gynecology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 4
Official FDA classification page: HGF
Classification and pathway per current FDA publications. Data from openFDA (CC0).