KXO
- Product code
- KXO
- Device name
- Monitor, Pressure, Intrauterine
- Device class
- Class 2
- 21 CFR
- 21 CFR 884.2700
- Medical specialty
- Obstetrics/Gynecology
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (all years, FDA)
- 26 (all years; only the last 3 years are listed here)
Official FDA classification page: KXO
Classification and pathway per current FDA publications. Data from openFDA (CC0).