Cleared Abbreviated

K172174 - Philips IntelliSite Pathology Solution (FDA 510(k) Clearance)

Oct 2017
Decision
77d
Days
Class 2
Risk

K172174 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 October 4, 2017, 77 days after receiving the submission on July 19, 2017.

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 K172174 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 19, 2017
Decision Date October 04, 2017
Days to Decision 77 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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