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Electrical Systems Div.

Country not established

Devices
1

What Electrical Systems Div. makes

The company produces the ESI Model MS-103, an electrical medical device designed for specific diagnostic or therapeutic applications within Class II categories.

This device is regulated under the FDA’s 510(k) pathway as a Class II product and is listed in the FDA’s 510(k) database. The manufacturer operates from 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

  • Esi Model Ms-103 Ref K885120

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

Frequently asked questions

How many devices does Electrical Systems Div. have in the registry?

The registry currently lists 1 device for Electrical Systems Div.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Electrical Systems Div.'s devices?

Among its 1 most recently registered device, Electrical Systems Div. has devices listed in FDA 510(k) (1 device).

What risk classes do Electrical Systems Div.'s devices fall under?

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

What are the newest devices from Electrical Systems Div. in the registry?

The most recently registered devices listed for Electrical Systems Div. include ESI MODEL MS-103.

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