Cleared Traditional

K233204 - Philips IntelliSite Pathology Solution 5.1 (FDA 510(k) Clearance)

Jun 2024
Decision
270d
Days
Class 2
Risk

K233204 is an FDA 510(k) clearance for the Philips IntelliSite Pathology Solution 5.1. This device is classified as a Whole Slide Imaging System (Class II - Special Controls, product code PSY).

Submitted by Philips Medical Systems Nederland B.V. (Best, NL). The FDA issued a Cleared decision on June 24, 2024, 270 days after receiving the submission on September 28, 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 K233204 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 28, 2023
Decision Date June 24, 2024
Days to Decision 270 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 9
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
Roche Digital Pathology Dx (VENTANA DP 200)
K232879 · Ventana Medical Systems, Inc. · Jun 2024
Philips IntelliSite Pathology Solution
K203845 · Philips Medical Systems Nederland B.V. · Sep 2021