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Fidus Medical Technology Corp.

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Devices
1

What Fidus Medical Technology Corp. makes

Fidus Medical Technology Corp. manufactures the RHYDER Diagnostic Catheter, a device designed for diagnostic procedures within the cardiovascular system.

The RHYDER Diagnostic Catheter is classified as a Class II medical device under FDA regulations and is listed via the 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

  • Rhyder Diagnostic Catheter Ref K962307

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

Frequently asked questions

How many devices does Fidus Medical Technology Corp. have in the registry?

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

Which registries list Fidus Medical Technology Corp.'s devices?

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

What risk classes do Fidus Medical Technology Corp.'s devices fall under?

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

What are the newest devices from Fidus Medical Technology Corp. in the registry?

The most recently registered devices listed for Fidus Medical Technology Corp. include RHYDER DIAGNOSTIC CATHETER.

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