IKZ
- Product code
- IKZ
- Device name
- Bed, Patient Rotation, Powered
- Device class
- Class 2
- 21 CFR
- 21 CFR 890.5225
- Medical specialty
- Physical Medicine
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 17 (all years; only the last 3 years are listed here)
Official FDA classification page: IKZ
Classification and pathway per current FDA publications. Data from openFDA (CC0).