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Imc

Country not established

Devices
1

What Imc makes

Imc manufactures the LIFELINE AMBULATORY, a portable device designed for continuous monitoring of cardiac rhythms and detection of arrhythmias during daily activities.

The LIFELINE AMBULATORY is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) clearance process. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Lifeline Ambulatory Ref K781054

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

Frequently asked questions

How many devices does Imc have in the registry?

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

Which registries list Imc's devices?

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

What risk classes do Imc's devices fall under?

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

What are the newest devices from Imc in the registry?

The most recently registered devices listed for Imc include LIFELINE AMBULATORY.

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