510(k) K240782 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
CellFX Percutaneous Electrode System (SYS3000); CellFX Percutaneous Electrode, 13G (CPE013); CellFX Percutaneous Electrode, 18G (CPE018)
| Applicant | Pulse Biosciences, Inc., Hayward CA, US |
| Decision | Substantially Equivalent, Aug 5, 2024 |
| Received | Mar 21, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240782
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.