K240311
- 510(k) number
- K240311
- Device name
- JETT Medical II
- Applicant
- Compex, Spol, S.R.O. CZ
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-01-22
- Date received
- 2024-02-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 1.6 MB · U.S. public domain
Also available from FDA: K240311.pdf
Official FDA record: K240311
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.