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Michael A Clark

Country not established

Devices
1

What Michael A Clark makes

Michael A Clark manufactures the ENDOXFLEX 5000, a device designed for endoscopic retrograde cholangiopancreatography (ERCP) procedures, specifically for biliary and pancreatic duct drainage.

The ENDOXFLEX 5000 is classified as a Class II medical device in the US and is listed under 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

  • Endoxflex 5000 Ref K946239

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

Frequently asked questions

How many devices does Michael A Clark have in the registry?

The registry currently lists 1 device for Michael A Clark. Devices recorded under merged duplicate company entries are counted once.

Which registries list Michael A Clark's devices?

Among its 1 most recently registered device, Michael A Clark has devices listed in FDA 510(k) (1 device).

What risk classes do Michael A Clark's devices fall under?

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

What are the newest devices from Michael A Clark in the registry?

The most recently registered devices listed for Michael A Clark include ENDOXFLEX 5000.

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