HEALTHWATCH

FDA Device Registration & Listing · Kfar Saba Central, IL · Registration 3010363430

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
3010363430
FEI Number
3010363430
Entity Name
HEALTHWATCH
City/State/Country
Kfar Saba Central, IL
Establishment Address
6 Hasadna Street, Kfar Saba Central 44424, IL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
HealthWatch (Owner Number: 10043447)
Owner / Operator Contact Address
23 Hataas Street, Kfar Saba, IL-M 4442500, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

MCC Master Caution Device MCD

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OUG Medical Device Data System General Hospital Class 1 880.6310 2014-11-27
DXH Transmitters And Receivers, Electrocardiograph, Telephone Cardiovascular Class 2 870.2920 2015-03-10

Official Correspondent

Yoram Levy

US Agent Details

Tova Rivnay Email: yoram@qsitemed.com Phone: (512) 5354930

Related Public Records

Same Entity

HealthWatch
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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3037966017 HEALTH DATA WORKS Ponte Vedra Beach, FL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010363430. Last updated year: 2026. Please use registration number 3010363430 when referencing this establishment in official correspondence.
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