Product code LHR
- Device name
- System, Thermographic, Liquid Crystal (Sole Diagnostic Screen)
- Medical specialty
- Obstetrics/Gynecology
- Device class
- 3
- Regulation number
- 884.2982
- Review panel
- RA
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset