IKO
- Product code
- IKO
- Device name
- Hammer, Reflex, Powered
- Device class
- Class 2
- 21 CFR
- 21 CFR 890.1450
- Medical specialty
- Physical Medicine
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 1
Official FDA classification page: IKO
Classification and pathway per current FDA publications. Data from openFDA (CC0).