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Van, Cott, Bagley, Cornwall & Mccarth

Country not established

Devices
1

What Van, Cott, Bagley, Cornwall & Mccarth makes

The company manufactures the Pulsetaker, a Class II medical device designed for monitoring or managing cardiac pulse waveforms in clinical settings.

The Pulsetaker is regulated under the FDA’s 510(k) pathway and is listed in the U.S. regulatory database. The manufacturer 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

  • Pulsetaker Ref K782131

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

Frequently asked questions

How many devices does Van, Cott, Bagley, Cornwall & Mccarth have in the registry?

The registry currently lists 1 device for Van, Cott, Bagley, Cornwall & Mccarth. Devices recorded under merged duplicate company entries are counted once.

Which registries list Van, Cott, Bagley, Cornwall & Mccarth's devices?

Among its 1 most recently registered device, Van, Cott, Bagley, Cornwall & Mccarth has devices listed in FDA 510(k) (1 device).

What risk classes do Van, Cott, Bagley, Cornwall & Mccarth's devices fall under?

Among its 1 most recently registered device, the classes recorded for Van, Cott, Bagley, Cornwall & Mccarth's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Van, Cott, Bagley, Cornwall & Mccarth in the registry?

The most recently registered devices listed for Van, Cott, Bagley, Cornwall & Mccarth include PULSETAKER.

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