HEJ
- Product code
- HEJ
- Device name
- Monitor, Hemic Sound, Ultrasonic
- Device class
- Class 2
- 21 CFR
- 21 CFR 884.2660
- Medical specialty
- Obstetrics/Gynecology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
Official FDA classification page: HEJ
Classification and pathway per current FDA publications. Data from openFDA (CC0).