Pulse Biosciences, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
Total Devices7
Categories1
Latest FDA decision2024-08-05
SEC Filings: 1 filings on record. Latest: 10-Q (2026-08-06). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K240782 | CellFX Percutaneous Electrode System (SYS3000); CellFX Percutaneous Electrode, 13G (CPE013); CellFX Percutaneous Electrode, 18G (CPE018) | GEI | 2024-08-05 | View |
| 510(k) | K233705 | CellFX Percutaneous Electrode System (SYS3000) | GEI | 2024-03-08 | View |
| 510(k) | K213674 | CellFX System | GEI | 2022-09-22 | View |
| 510(k) | K222075 | CellFX System | GEI | 2022-09-02 | View |
| 510(k) | K221671 | CellFX® System | GEI | 2022-08-01 | View |
| 510(k) | K211444 | CellFX System | GEI | 2021-08-25 | View |
| 510(k) | K203299 | CellFX System | GEI | 2021-02-02 | View |
No matching devices.