K243139
- 510(k) number
- K243139
- Device name
- Reverso Pro System
- Applicant
- Indiba S. A. U. ES
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-01-22
- Date received
- 2024-09-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 3.0 MB · U.S. public domain
Also available from FDA: K243139.pdf
Official FDA record: K243139
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.