HDE
- Product code
- HDE
- Device name
- Hook, Fibroid, Gynecological
- Device class
- Class 1
- 21 CFR
- 21 CFR 884.4520
- Medical specialty
- Obstetrics/Gynecology
- Marketing pathway
- 510(K) Exempt
Official FDA classification page: HDE
Classification and pathway per current FDA publications. Data from openFDA (CC0).