LLE
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Stimulator, Spinal-Cord, Implanted For Peripheral Vascular Disease
- Device class
- Class III (high risk)
- Medical specialty
- Unknown
- Flags
- Implant
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| BLOOD GAS EXPERSYSTEM 8700 (K833430) | Medical Intelcom, Inc. | 1984-02-10 |
| INIVOX ELECTRODE/CATHETER SYS (K832916) | Critikon Company, LLC | 1983-11-14 |
Track LLE automatically
Every clearance here is in the API, with alerts when new ones post.