K233705
- 510(k) number
- K233705
- Device name
- CellFX Percutaneous Electrode System (SYS3000)
- Applicant
- Pulse Biosciences, Inc. CA · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-03-08
- Date received
- 2023-11-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K233705.pdf
Official FDA record: K233705
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.