IKN
- Product code
- IKN
- Device name
- Electromyograph, Diagnostic
- Device class
- Class 2
- 21 CFR
- 21 CFR 890.1375
- Medical specialty
- Physical Medicine
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 75
Official FDA classification page: IKN
Classification and pathway per current FDA publications. Data from openFDA (CC0).