Cleared Traditional

Philips IntelliSite Pathology Solution 5.1

K233204 · Philips Medical Systems Nederland B.V. · Pathology

Jun 2024

Decision

270d

Days

Class 2

Risk

About This 510(k) Submission

K233204 is an FDA 510(k) clearance for the Philips IntelliSite Pathology Solution 5.1, 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 review panel. Regulated under 21 CFR 864.3700.

Submission Details

510(k) Number	K233204 FDA.gov
FDA Decision	Cleared 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).