Neuromodulatory Devices & Applications
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K251210 | Ampa One System (AMPA-001) | June 27, 2025 |
| K243319 | Ampa One System (AMPA-001) | February 13, 2025 |