K253176
- 510(k) number
- K253176
- Device name
- TearView
- Applicant
- Beyond 700 Pty, Ltd. AU
- Product code
- HKI — Camera, Ophthalmic, Ac-Powered
- Decision date
- 2026-06-22
- Date received
- 2025-09-26
- 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: K253176.pdf
Official FDA record: K253176
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.