PATHPRESENTER CORP

FDA Device Registration & Listing · Montville, NJ, US · Registration 3039498387

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3039498387
FEI Number
3039498387
Entity Name
PATHPRESENTER CORP
City/State/Country
Montville, NJ, US
Establishment Address
19 Louis Dr, Montville, NJ 07045, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
PathPresenter (Owner Number: 10093699)
Owner / Operator Contact Address
19 Louis Drive, Montville, NJ 07045, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K250968
PMA Number
N/A

All Registered Proprietary Names

PathPresenter Clinical Viewer

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QKQ Digital Pathology Image Viewing And Management Software Pathology Class 2 864.3700 2025-08-07

Official Correspondent

Brian Matcheski

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PathPresenter
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3039498387. Last updated year: 2026. Please use registration number 3039498387 when referencing this establishment in official correspondence.
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