K240303
- 510(k) number
- K240303
- Device name
- MetaLite DX Digital Pathology Software
- Applicant
- Jellox Biotech, Inc. TW
- Product code
- QKQ — Digital Pathology Image Viewing And Management Softw
- Decision date
- 2024-10-28
- Date received
- 2024-02-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Pathology
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K240303.pdf
Official FDA record: K240303
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.