LQK
- Product code
- LQK
- Device name
- Home Uterine Activity Monitor
- Device class
- Class 2
- 21 CFR
- 21 CFR 884.2730
- Medical specialty
- Obstetrics/Gynecology
- Marketing pathway
- 510(K)
- 510(k) clearances (all years, FDA)
- 5 (all years; only the last 3 years are listed here)
Official FDA classification page: LQK
Classification and pathway per current FDA publications. Data from openFDA (CC0).