KXH
- Product code
- KXH
- Device name
- Cradle, Patient, Radiologic
- Device class
- Class 1
- 21 CFR
- 21 CFR 892.1830
- Medical specialty
- Radiology
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 9
Official FDA classification page: KXH
Classification and pathway per current FDA publications. Data from openFDA (CC0).