K252979
- 510(k) number
- K252979
- Device name
- Voyager DSLT (430840610)
- Applicant
- Belkin Vision, Ltd. IL
- Product code
- HQF — Laser, Ophthalmic
- Decision date
- 2026-04-07
- Date received
- 2025-09-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ophthalmic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K252979.pdf
Official FDA record: K252979
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.