K231971
- 510(k) number
- K231971
- Device name
- DEKA PHYSIQ 360
- Applicant
- El.En S.P.A. IT
- Product code
- PKT — Laser For Disruption Of Adipocyte Cells For Aestheti
- Decision date
- 2023-09-26
- Date received
- 2023-07-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K231971.pdf
Official FDA record: K231971
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.