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Aftercal, Inc.

Country not established

Devices
1

What Aftercal, Inc. makes

Aftercal, Inc. manufactures pneumotachography systems, which measure airflow in respiratory studies to assess lung function and ventilation efficiency.

These devices are classified as Class I under FDA regulations and are 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

  • Pneumotachography System Ref K760816

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

Frequently asked questions

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

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

Which registries list Aftercal, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Aftercal, Inc. include PNEUMOTACHOGRAPHY SYSTEM.

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