HFM
- Product code
- HFM
- Device name
- Monitor, Uterine Contraction, External (For Use In Clinic)
- Device class
- Class 2
- 21 CFR
- 21 CFR 884.2720
- Medical specialty
- Obstetrics/Gynecology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 23
Official FDA classification page: HFM
Classification and pathway per current FDA publications. Data from openFDA (CC0).