K232202
- 510(k) number
- K232202
- Device name
- Aperio GT 450 DX
- Applicant
- Leica Biosystems Imaging, Inc. CA · US
- Product code
- PSY — Whole Slide Imaging System
- Decision date
- 2024-04-16
- Date received
- 2023-07-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Pathology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K232202.pdf
Official FDA record: K232202
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.