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Washington Biolab, Inc.

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Devices
1

What Washington Biolab, Inc. makes

Washington Biolab, Inc. manufactures the Washington Cardiac Monitor, a device designed for continuous or intermittent electrocardiogram (ECG) monitoring to assess cardiac activity and detect arrhythmias.

The company’s portfolio is regulated under Class II devices in the US, with the Washington Cardiac Monitor authorised via the FDA’s 510(k) clearance process. The manufacturer 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

  • Washington Cardiac Monitor Ref K903710

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

Frequently asked questions

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

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

Which registries list Washington Biolab, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Washington Biolab, Inc. include WASHINGTON CARDIAC MONITOR.

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