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Cardiac Telecom Corp.

United StatesFDA applicant, unverified

Devices
2

What Cardiac Telecom Corp. makes

Cardiac Telecom Corp. manufactures the Heartlink Model II and the Heartrac ECG monitoring system. These devices are designed for cardiac monitoring applications.

The company is based in the United States, and its portfolio consists of Class II medical devices. These products are listed in the FDA 510(k) regulatory registry.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Heartlink, Model Ii Ref K982803

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Heartrac Ecg Monitoring System Ref K934913

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Cardiac Telecom Corp. have in the registry?

The registry currently lists 2 devices for Cardiac Telecom Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cardiac Telecom Corp.'s devices?

Among its 2 most recently registered devices, Cardiac Telecom Corp. has devices listed in FDA 510(k) (2 devices).

What risk classes do Cardiac Telecom Corp.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Cardiac Telecom Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Cardiac Telecom Corp. in the registry?

The most recently registered devices listed for Cardiac Telecom Corp. include HEARTLINK, MODEL II and HEARTRAC ECG MONITORING SYSTEM.

Generated automatically from registry data and not verified by a human reviewer.