MOH
- Product code
- MOH
- Device name
- Monitor, Heart Rate, Fetal, Non-Stress Test (Home Use)
- Device class
- Class 2
- 21 CFR
- 21 CFR 884.2730
- Medical specialty
- Obstetrics/Gynecology
- Marketing pathway
- 510(K)
Official FDA classification page: MOH
Classification and pathway per current FDA publications. Data from openFDA (CC0).