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Credo

South KoreaFDA 510(k) applicant, unverified

Devices
1

What Credo makes

Credo manufactures the CPR BAND, a Class II medical device.

The company is based in the US and its devices are listed in the FDA 510(k) registry.

AI-generated from registry data, 22 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Cpr Band Ref K201581

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

Frequently asked questions

How many devices does Credo have in the registry?

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

Which registries list Credo's devices?

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

What risk classes do Credo's devices fall under?

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

What are the newest devices from Credo in the registry?

The most recently registered devices listed for Credo include CPR BAND.

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