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Kenneth J. Purcell

Country not established

Devices
1

What Kenneth J. Purcell makes

Kenneth J. Purcell manufactures the Electro-Acuscope, a device used for diagnostic evaluation of muscle and nerve function through electrical impedance measurements.

The Electro-Acuscope is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. 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

  • Electro-Acuscope Ref K832442

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

Frequently asked questions

How many devices does Kenneth J. Purcell have in the registry?

The registry currently lists 1 device for Kenneth J. Purcell. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kenneth J. Purcell's devices?

Among its 1 most recently registered device, Kenneth J. Purcell has devices listed in FDA 510(k) (1 device).

What risk classes do Kenneth J. Purcell's devices fall under?

Among its 1 most recently registered device, the classes recorded for Kenneth J. Purcell's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Kenneth J. Purcell in the registry?

The most recently registered devices listed for Kenneth J. Purcell include ELECTRO-ACUSCOPE.

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