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Nhe Corp.

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Devices
1

What Nhe Corp. makes

Nhe Corp. manufactures the PE 501 PC-ECG Monitor, a device designed for continuous electrocardiogram (ECG) monitoring to record and display heart activity.

The PE 501 PC-ECG Monitor is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Pe 501 Pc-Ecg Monitor Ref K992584

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

Frequently asked questions

How many devices does Nhe Corp. have in the registry?

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

Which registries list Nhe Corp.'s devices?

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

What risk classes do Nhe Corp.'s devices fall under?

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

What are the newest devices from Nhe Corp. in the registry?

The most recently registered devices listed for Nhe Corp. include PE 501 PC-ECG MONITOR.

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