K240504
- 510(k) number
- K240504
- Device name
- PLASMA EDGE System
- Applicant
- Lamidey Noury Medical FR
- Product code
- FAS — Electrode, Electrosurgical, Active, Urological
- Decision date
- 2024-06-12
- Date received
- 2024-02-21
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K240504.pdf
Official FDA record: K240504
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.