K260647
- 510(k) number
- K260647
- Device name
- SPECCHIO
- Applicant
- El.En S.P.A. IT
- Product code
- PBX — Massager, Vacuum, Radio Frequency Induced Heat
- Decision date
- 2026-04-02
- Date received
- 2026-02-27
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K260647.pdf
Official FDA record: K260647
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.