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Catheter Corp. of America

Country not established

Devices
1

What Catheter Corp. of America makes

Catheter Corp. of America manufactures thermal dilution catheters, which are used for measuring cardiac output and assessing hemodynamic function in clinical settings.

These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Thermal Dilution Catheter Ref K832324

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

Frequently asked questions

How many devices does Catheter Corp. of America have in the registry?

The registry currently lists 1 device for Catheter Corp. of America. Devices recorded under merged duplicate company entries are counted once.

Which registries list Catheter Corp. of America's devices?

Among its 1 most recently registered device, Catheter Corp. of America has devices listed in FDA 510(k) (1 device).

What risk classes do Catheter Corp. of America's devices fall under?

Among its 1 most recently registered device, the classes recorded for Catheter Corp. of America's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Catheter Corp. of America in the registry?

The most recently registered devices listed for Catheter Corp. of America include THERMAL DILUTION CATHETER.

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