K240070
- 510(k) number
- K240070
- Device name
- Profound Matrix
- Applicant
- Candela Corporation MA · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-07-01
- Date received
- 2024-01-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K240070.pdf
Official FDA record: K240070
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.