K242508
- 510(k) number
- K242508
- Device name
- Verily Numetric Retinal Camera
- Applicant
- Verily Life Sciences, LLC CA · US
- Product code
- HKI — Camera, Ophthalmic, Ac-Powered
- Decision date
- 2024-12-09
- Date received
- 2024-08-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- Ophthalmic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K242508.pdf
Official FDA record: K242508
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.