KQW
- Product code
- KQW
- Device name
- Goniometer, Nonpowered
- Device class
- Class 1
- 21 CFR
- 21 CFR 888.1520
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 13
Official FDA classification page: KQW
Classification and pathway per current FDA publications. Data from openFDA (CC0).