K251952
- 510(k) number
- K251952
- Device name
- Virasight
- Applicant
- Virasoft Corporation NY · US
- Product code
- PSY — Whole Slide Imaging System
- Decision date
- 2026-07-17
- Date received
- 2025-06-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Pathology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K251952.pdf
Official FDA record: K251952
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.