Cleared Abbreviated

K203845 - Philips IntelliSite Pathology Solution (FDA 510(k) Clearance)

Sep 2021
Decision
260d
Days
Class 2
Risk

K203845 is an FDA 510(k) clearance for the Philips IntelliSite Pathology Solution. 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 September 17, 2021, 260 days after receiving the submission on December 31, 2020.

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 K203845 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 31, 2020
Decision Date September 17, 2021
Days to Decision 260 days
Submission Type Abbreviated
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).

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