Pulse Biosciences, Inc.
Pulse Biosciences, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Aug 5, 2024.
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 | Aug 5, 2024 |
| K233705 | CellFX Percutaneous Electrode System (SYS3000) | Mar 8, 2024 |
| K213674 | CellFX System | Sep 22, 2022 |
| K222075 | CellFX System | Sep 2, 2022 |
| K221671 | CellFX® System | Aug 1, 2022 |
| K211444 | CellFX System | Aug 25, 2021 |
| K203299 | CellFX System | Feb 2, 2021 |