510(k) K233705 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
CellFX Percutaneous Electrode System (SYS3000)
| Applicant | Pulse Biosciences, Inc., Hayward CA, US |
| Decision | Substantially Equivalent, Mar 8, 2024 |
| Received | Nov 20, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233705
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.