K261833
- 510(k) number
- K261833
- Device name
- NEUROMARK System (NMK00301)
- Applicant
- Neurent Medical , Ltd. IE
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2026-06-16
- Date received
- 2026-06-02
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K261833.pdf
Official FDA record: K261833
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.