Cleared Traditional

K230839 - Concentriq Dx (FDA 510(k) Clearance)

Feb 2024
Decision
318d
Days
Class 2
Risk

K230839 is an FDA 510(k) clearance for the Concentriq Dx. This device is classified as a Whole Slide Imaging System (Class II - Special Controls, product code PSY).

Submitted by Proscia, Inc. (Philadelphia, US). The FDA issued a Cleared decision on February 8, 2024, 318 days after receiving the submission on March 27, 2023.

This device falls under the Pathology FDA review panel. Regulated under 21 CFR 864.3700. The Whole Slide Imaging System Is An Automated Digital Slide Creation, Viewing, And Management System Intended As An Aid To The Pathologist To Review And Interpret Digital Images Of Surgical Pathology Slides Prepared From Formalin-fixed, Paraffin-embedded (ffpe) Tissue. The System Generates Digital Images That Would Otherwise Be Appropriate For Manual Visualization By Conventional Brightfield Microscopy. The Whole Slide Imaging System Is Not Intended For Use With Slides Prepared From Frozen Tissue, Cytology, And Non-ffpe Hematopathology Specimens (e.g., Peripheral Blood Smear)..

Submission Details

510(k) Number K230839 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 27, 2023
Decision Date February 08, 2024
Days to Decision 318 days
Submission Type Traditional
Review Panel Pathology (PA)
Summary Summary PDF

Device Classification

Product Code PSY - Whole Slide Imaging System
Device Class Class II - Special Controls
CFR Regulation 21 CFR 864.3700
Definition The Whole Slide Imaging System Is An Automated Digital Slide Creation, Viewing, And Management System Intended As An Aid To The Pathologist To Review And Interpret Digital Images Of Surgical Pathology Slides Prepared From Formalin-fixed, Paraffin-embedded (ffpe) Tissue. The System Generates Digital Images That Would Otherwise Be Appropriate For Manual Visualization By Conventional Brightfield Microscopy. The Whole Slide Imaging System Is Not Intended For Use With Slides Prepared From Frozen Tissue, Cytology, And Non-ffpe Hematopathology Specimens (e.g., Peripheral Blood Smear).

Similar Devices - PSY Whole Slide Imaging System

All 10
Philips IntelliSite Pathology Solution 5.1
K243871 · Philips Medical Systems Nederland B.V. · Mar 2025
Roche Digital Pathology Dx
K242783 · Ventana Medical Systems, Inc. · Dec 2024
Philips IntelliSite Pathology Solution 5.1
K242848 · Philips Medical Systems Nederland B.V. · Dec 2024
Philips IntelliSite Pathology Solution
K241871 · Philips Medical Systems Nederland B.V. · Dec 2024
Philips IntelliSite Pathology Solution 5.1
K233204 · Philips Medical Systems Nederland B.V. · Jun 2024
Roche Digital Pathology Dx (VENTANA DP 200)
K232879 · Ventana Medical Systems, Inc. · Jun 2024