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A.R. Nelson Co., Inc.

Country not established

Devices
1

What A.R. Nelson Co., Inc. makes

A.R. Nelson Co., Inc. manufactures the ARNCO I.V. Monitor, a device designed for intravenous fluid administration monitoring to ensure accurate infusion rates and patient safety.

The ARNCO I.V. Monitor is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. 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

  • Arnco I.V. Monitor Ref K760694

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does A.R. Nelson Co., Inc. have in the registry?

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

Which registries list A.R. Nelson Co., Inc.'s devices?

Among its 1 most recently registered device, A.R. Nelson Co., Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do A.R. Nelson Co., Inc.'s devices fall under?

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

What are the newest devices from A.R. Nelson Co., Inc. in the registry?

The most recently registered devices listed for A.R. Nelson Co., Inc. include ARNCO I.V. MONITOR.

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