Pulse Biosciences, Inc. · Class II · Cleared Aug 5, 2024
| K-number | K240782 |
| Device name | CellFX Percutaneous Electrode System (SYS3000); CellFX Percutaneous Electrode, 13G (CPE013); CellFX Percutaneous Electrode, 18G (CPE018) |
| Applicant | Pulse Biosciences, Inc. |
| Product code | GEI |
| Device class | Class II |
| Decision date | Aug 5, 2024 |
| Decision | Substantially Equivalent |
| Regulation | 878.4400 |
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