K232051
- 510(k) number
- K232051
- Device name
- VISULAS green
- Applicant
- Carl Zeiss Meditec CA · US
- Product code
- HQF — Laser, Ophthalmic
- Decision date
- 2023-10-24
- Date received
- 2023-07-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ophthalmic
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K232051.pdf
Official FDA record: K232051
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.