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Mcg, Inc.

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Devices
1

What Mcg, Inc. makes

McG, Inc. manufactures the Electroapplicator Model C-1, a device designed for controlled electrical stimulation applications in medical settings.

The Electroapplicator Model C-1 is classified as a Class II device under FDA regulations and is listed via the 510(k) clearance process. 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

  • Electroapplicator Model C-1 Ref K790205

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

Frequently asked questions

How many devices does Mcg, Inc. have in the registry?

The registry currently lists 1 device for Mcg, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Mcg, Inc.'s devices?

Among its 1 most recently registered device, Mcg, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Mcg, Inc.'s devices fall under?

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

What are the newest devices from Mcg, Inc. in the registry?

The most recently registered devices listed for Mcg, Inc. include ELECTROAPPLICATOR MODEL C-1.

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