LHR
- Product code
- LHR
- Device name
- System, Thermographic, Liquid Crystal (Sole Diagnostic Screen)
- Device class
- Class 3
- 21 CFR
- 21 CFR 884.2982
- Medical specialty
- Obstetrics/Gynecology
- Marketing pathway
- PMA
Official FDA classification page: LHR
Classification and pathway per current FDA publications. Data from openFDA (CC0).