IKO
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Hammer, Reflex, Powered
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 890.1450
- Medical specialty
- Physical Medicine
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| OPERATIVE RECORDING CAMERA (K904113) | Medical Dynamics, Inc. | 1990-10-30 |
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