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Arzco Medical Electronics, Inc.

United StatesFDA applicant, unverified

Devices
3

What Arzco Medical Electronics, Inc. makes

Arzco Medical Electronics, Inc. manufactures esophageal cardiac recording devices, including stethoscopes and catheters designed for intracardiac electrophysiological monitoring. These products capture electrical signals from the esophagus to aid in diagnosing arrhythmias and cardiac conditions. The portfolio includes both stethoscope-based and catheter-based recording systems, each equipped with multiple electrodes for precise signal acquisition.

The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. These products are listed in the FDA’s 510(k) database, adhering to U.S. medical device compliance standards. The manufacturer operates from the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

Frequently asked questions

How many devices does Arzco Medical Electronics, Inc. have in the registry?

The registry currently lists 3 devices for Arzco Medical Electronics, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Arzco Medical Electronics, Inc.'s devices?

Among its 3 most recently registered devices, Arzco Medical Electronics, Inc. has devices listed in FDA 510(k) (3 devices).

What risk classes do Arzco Medical Electronics, Inc.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Arzco Medical Electronics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Arzco Medical Electronics, Inc. in the registry?

The most recently registered devices listed for Arzco Medical Electronics, Inc. include TAPSCOPE ESOPHAGEAL CARDIAC RECORDING STETHOSCOPE, ARZO TAPCATH ESOPHAGEAL RECORDING CATHETER and ARZCO OCTAPOLAR ESOPHAGEAL CARDIAC RECORD CATH.

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