K233237
- 510(k) number
- K233237
- Device name
- xeo+ Family
- Applicant
- Cutera, Inc. CA · US
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2023-12-15
- Date received
- 2023-09-28
- 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: K233237.pdf
Official FDA record: K233237
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.