LQK
2026-09-03
Home Uterine Activity Monitor
FDA product code LQK · 5 cleared devices
Class 2
Obstetrics/Gynecology
- Regulation
- 21 CFR 884.2730
- Review panel
- OB
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 2002-04-19 – 2026-09-03
LQK
2022-05-06
Invu by Nuvo
View details →
LQK
2021-05-28
INVU by Nuvo
View details →
LQK
2020-03-27
PregSense
View details →
LQK
2002-04-19
MODIFICATION TO FETAL ASSIST
View details →No matching devices.
Advertisement