KITRON TECHNOLOGIES INC.

FDA Device Registration & Listing · Windber, PA, US · Registration 3017884848

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
3017884848
FEI Number
3017884848
Entity Name
KITRON TECHNOLOGIES INC.
City/State/Country
Windber, PA, US
Establishment Address
345 Pomroys Dr, Windber, PA 15963, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Kitron Technologies Inc. (Owner Number: 10095470)
Owner / Operator Contact Address
345 Pomroys Drive, Windber, PA 15963, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HeartBeam AIMIGo with 12-L ECG Synthesis Software System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DXH Transmitters And Receivers, Electrocardiograph, Telephone Cardiovascular Class 2 870.2920 2026-03-17

Official Correspondent

Clayton Watson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Kitron Technologies 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
K820986 Dart Medical Equipment EKG MONITORS, VARIOUS MODELS 1982-04-29
K910450 Medtech Industries, Inc. CARD GUARD-3000 ECG TELEPHONE ADAPTER 1991-05-07
K761318 Cambridge Instruments, Inc. 3038 OPTION B-COMPUT. TRANS. TERMINAL 1977-01-06
K972649 Reynolds Medical , Ltd. CARDIOCALL CARDIAC EVENT RECORDER 1997-12-04
K033410 Remote Diagnostic Technologies , Ltd. TEMPUS 2000 PATIENT MONITOR, MODEL 00-0002 2004-03-05

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017884848. Last updated year: 2026. Please use registration number 3017884848 when referencing this establishment in official correspondence.
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