FOGG SYSTEM COMPANY, INC.

FDA Device Registration & Listing · Aurora, CO, US · Registration 3001762454

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
3001762454
FEI Number
3001762454
Entity Name
FOGG SYSTEM COMPANY, INC.
City/State/Country
Aurora, CO, US
Establishment Address
15592 East Batavia Dr, Aurora, CO 80011, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Fogg System Company, Inc. (Owner Number: 10089301)
Owner / Operator Contact Address
15592 East Batavia Dr, Aurora, CO 80011, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K222712
PMA Number
N/A

All Registered Proprietary Names

Fogg System Patient Monitoring Cables

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DSA Cable, Transducer And Electrode, Patient, (Including Connector) Cardiovascular Class 2 870.2900 2023-11-27

Official Correspondent

Caroline Rovere

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Fogg System Company, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K880323 Medtronic Vascular MEDTRONIC MODEL 5411 SURGICAL CABLE ADAPTOR 1988-03-22

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3001762454. Last updated year: 2026. Please use registration number 3001762454 when referencing this establishment in official correspondence.
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