Product code LQK
- Device name
- Home Uterine Activity Monitor
- Medical specialty
- Obstetrics/Gynecology
- Device class
- 2
- Regulation number
- 884.2730
- Review panel
- OB
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Ineligible
- Source
- FDA openFDA device classification dataset