K261380
- 510(k) number
- K261380
- Device name
- Concentriq AP-Dx
- Applicant
- Proscia, Inc. PA · US
- Product code
- QKQ — Digital Pathology Image Viewing And Management Softw
- Decision date
- 2026-08-05
- Date received
- 2026-04-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Pathology
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K261380.pdf
Official FDA record: K261380
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.