Skip to content

Riko Medical & Scientific Instrument Corp.

United StatesFDA applicant, unverified

Devices
3

What Riko Medical & Scientific Instrument Corp. makes

Riko Medical & Scientific Instrument Corp. manufactures spirometry devices, including the SPIROMATE AS-500 and SPIROMATE AS-600, which measure lung function and airflow metrics. The company also produces a plotter accessory designed for use with the AS-500 model to generate printed respiratory test reports.

These devices are classified as Class II under FDA regulations and are listed in the FDA 510(k) database. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Spiromate As-500 Ref K842372

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Plotter For As-500 Ref K853922

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Spiromate As-600 Ref K862023

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

Frequently asked questions

How many devices does Riko Medical & Scientific Instrument Corp. have in the registry?

The registry currently lists 3 devices for Riko Medical & Scientific Instrument Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Riko Medical & Scientific Instrument Corp.'s devices?

Among its 3 most recently registered devices, Riko Medical & Scientific Instrument Corp. has devices listed in FDA 510(k) (3 devices).

What risk classes do Riko Medical & Scientific Instrument Corp.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Riko Medical & Scientific Instrument Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Riko Medical & Scientific Instrument Corp. in the registry?

The most recently registered devices listed for Riko Medical & Scientific Instrument Corp. include SPIROMATE AS-500, PLOTTER FOR AS-500 and SPIROMATE AS-600.

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