KQX
- Product code
- KQX
- Device name
- Goniometer, Ac-Powered
- Device class
- Class 1
- 21 CFR
- 21 CFR 888.1500
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 33 (all years; only the last 3 years are listed here)
Official FDA classification page: KQX
Classification and pathway per current FDA publications. Data from openFDA (CC0).