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Karl M. Block Co.

Country not established

Devices
1

What Karl M. Block Co. makes

Karl M. Block Co. manufactures the KEITH-A.R.V., a device designed for measuring and monitoring arterial blood pressure in clinical settings, particularly for assessing vascular resistance and cardiac function.

The KEITH-A.R.V. is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Keith-A.R.V. Ref K851444 Open recall

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

Frequently asked questions

How many devices does Karl M. Block Co. have in the registry?

The registry currently lists 1 device for Karl M. Block Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Karl M. Block Co.'s devices?

Among its 1 most recently registered device, Karl M. Block Co. has devices listed in FDA 510(k) (1 device).

What risk classes do Karl M. Block Co.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Karl M. Block Co.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Karl M. Block Co. in the registry?

The most recently registered devices listed for Karl M. Block Co. include KEITH-A.R.V..

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