K230839
- 510(k) number
- K230839
- Device name
- Concentriq Dx
- Applicant
- Proscia, Inc. PA · US
- Product code
- PSY — Whole Slide Imaging System
- Decision date
- 2024-02-08
- Date received
- 2023-03-27
- 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: K230839.pdf
Official FDA record: K230839
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.