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Baker & Hostetler

Country not established

Devices
1

What Baker & Hostetler makes

Baker & Hostetler manufactures intravenous (I.V.) administration sets, which are sterile, single-use devices designed for the delivery of fluids, medications, or nutrients directly into a patient’s bloodstream.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company’s products are registered in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • I.V. Administration Set Ref K822027

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

Frequently asked questions

How many devices does Baker & Hostetler have in the registry?

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

Which registries list Baker & Hostetler's devices?

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

What risk classes do Baker & Hostetler's devices fall under?

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

What are the newest devices from Baker & Hostetler in the registry?

The most recently registered devices listed for Baker & Hostetler include I.V. ADMINISTRATION SET.

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