IKT
- Product code
- IKT
- Device name
- Electrode, Needle, Diagnostic Electromyograph
- Device class
- Class 2
- 21 CFR
- 21 CFR 890.1385
- Medical specialty
- Physical Medicine
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
- 510(k) clearances (last 3 years)
- 43
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K253581 | 2026-03-15 | Technomed Europe | Disposable Concentric Needle Electrode 0.30x25mm Red |
Official FDA classification page: IKT
Classification and pathway per current FDA publications. Data from openFDA (CC0).