LHP
- Product code
- LHP
- Device name
- System, Telethermographic (Sole Diagnostic Screen)
- Device class
- Class 3
- 21 CFR
- 21 CFR 884.2980
- Medical specialty
- Obstetrics/Gynecology
- Marketing pathway
- PMA
Official FDA classification page: LHP
Classification and pathway per current FDA publications. Data from openFDA (CC0).