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Quicksilver Systems, Inc.

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Devices
1

What Quicksilver Systems, Inc. makes

Quicksilver Systems, Inc. manufactures the QUICK READ 2000 (QR2000), a portable device designed for rapid diagnostic testing in point-of-care settings.

The QR2000 is classified as a Class I medical device 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

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Frequently asked questions

How many devices does Quicksilver Systems, Inc. have in the registry?

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

Which registries list Quicksilver Systems, Inc.'s devices?

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

What risk classes do Quicksilver Systems, Inc.'s devices fall under?

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

What are the newest devices from Quicksilver Systems, Inc. in the registry?

The most recently registered devices listed for Quicksilver Systems, Inc. include QUICK READ 2000 (QR2000).

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