Latest News: Proscia Receives FDA 510(k) Clearance For Concentriq AP-DxREAD THE PRESS RELEASE

Concentriq® AP-Dx is a comprehensive solution for primary diagnosis that immerses pathologists in an intuitive experience for viewing, interpreting, sharing and managing whole slide images. Designed for clinical settings of all sizes — from individual reference laboratories to the largest hospital systems — it helps drive confidence and efficiency gains.

Proscia receives FDA 510(k) clearance for Concentriq® AP-Dx

Proscia has received 510(k) clearance from the United States (U.S.) Food and Drug Administration (FDA) for Concentriq AP-Dx. The digital pathology solution was cleared for the purpose of primary diagnosis.

READ THE PRESS RELEASE

On-Demand Webinar

Welcome to Concentriq AP-Dx

See how you can change the future of your lab

Watch this webinar for an interactive demonstration of Concentriq AP-Dx, our digital pathology solution cleared by the U.S. FDA (K230839) for the purpose of primary diagnosis.

Learn about the multi-site clinical study Proscia conducted in support of our 510(k) clearance, and watch a product demo where we showcase the pathologist-centric design of Concentriq AP-Dx featuring workflows built for the modern AP lab:

  • Real-time collaboration with colleagues to broaden access to expertise
  • Performant viewer and tools for an easy transition to digital
  • Interoperability to support large, multi-site organizations

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For labs ready to accelerate their shift to 100% digital, go forward in confidence with Proscia. We provide solutions and professional services for every lab seeking to improve quality, run more efficiently and be positioned for future growth.

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PathGroup CMO Derek C. Welch, MD, FCAP

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