Pulse Biosciences, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K240782 | CellFX Percutaneous Electrode System (SYS3000); CellFX Percutaneous Electrode, 13G (CPE013); CellFX | August 5, 2024 |
| K233705 | CellFX Percutaneous Electrode System (SYS3000) | March 8, 2024 |
| K213674 | CellFX System | September 22, 2022 |
| K222075 | CellFX System | September 2, 2022 |
| K221671 | CellFX® System | August 1, 2022 |
| K211444 | CellFX System | August 25, 2021 |
| K203299 | CellFX System | February 2, 2021 |