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Respiration Technology, Inc.

Country not established

Devices
1

What Respiration Technology, Inc. makes

Respiration Technology, Inc. manufactures the AUTO PRO, a device designed for respiratory support and ventilation in clinical settings.

The company’s portfolio is regulated under FDA Class II devices, with the AUTO PRO authorised via the 510(k) pathway. The company 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

  • Auto Pro Ref K853378

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

Frequently asked questions

How many devices does Respiration Technology, Inc. have in the registry?

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

Which registries list Respiration Technology, Inc.'s devices?

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

What risk classes do Respiration Technology, Inc.'s devices fall under?

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

What are the newest devices from Respiration Technology, Inc. in the registry?

The most recently registered devices listed for Respiration Technology, Inc. include AUTO PRO.

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