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E For M Imaging Systems Div., Marquette Electronic

Country not established

Devices
2

What E For M Imaging Systems Div., Marquette Electronic makes

E For M Imaging Systems Div. manufactures electrophysiology (EPS) systems for cardiac mapping and ablation procedures, as well as intracardiac echocardiography (ICE) catheters like the ACCULUPE line. These devices support real-time visualization and guidance during electrophysiological studies and catheter ablation therapies.

The company’s products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. The portfolio is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Eps Ref K974504

    Class II
    Active 510(k) 510(k) II
  • Acculupe Ref K955184

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

How many devices does E For M Imaging Systems Div., Marquette Electronic have in the registry?

The registry currently lists 2 devices for E For M Imaging Systems Div., Marquette Electronic. Devices recorded under merged duplicate company entries are counted once.

Which registries list E For M Imaging Systems Div., Marquette Electronic's devices?

Among its 2 most recently registered devices, E For M Imaging Systems Div., Marquette Electronic has devices listed in FDA 510(k) (2 devices).

What risk classes do E For M Imaging Systems Div., Marquette Electronic's devices fall under?

Among its 2 most recently registered devices, the classes recorded for E For M Imaging Systems Div., Marquette Electronic's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from E For M Imaging Systems Div., Marquette Electronic in the registry?

The most recently registered devices listed for E For M Imaging Systems Div., Marquette Electronic include EPS and ACCULUPE.

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