K230722
- 510(k) number
- K230722
- Device name
- Eagle device
- Applicant
- Belkin Vision, Ltd. IL
- Product code
- HQF — Laser, Ophthalmic
- Decision date
- 2023-12-08
- Date received
- 2023-03-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ophthalmic
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K230722.pdf
Official FDA record: K230722
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.