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The Rupp & Bowman Co.

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Devices
3

What The Rupp & Bowman Co. makes

The Rupp & Bowman Co. manufactures laboratory instruments for clinical chemistry, including calcium measurement devices like the KONE Calcium Test and multi-parameter analyzers such as the Specific Chemistry Analyzer and Microlyte 7. These products are designed for in vitro diagnostic use to analyze blood and serum samples for electrolyte and metabolic markers.

The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with submissions recorded in the FDA’s 510(k) clearance registry. These instruments are intended for use in clinical laboratories and are governed by the U.S. Food and Drug Administration’s regulatory framework.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Kone Calcium Test Ref K880242

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Specific Chemistry Analyzer Ref K882081

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Microlyte 7 Ref K880973

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

Frequently asked questions

How many devices does The Rupp & Bowman Co. have in the registry?

The registry currently lists 3 devices for The Rupp & Bowman Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list The Rupp & Bowman Co.'s devices?

Among its 3 most recently registered devices, The Rupp & Bowman Co. has devices listed in FDA 510(k) (3 devices).

What risk classes do The Rupp & Bowman Co.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for The Rupp & Bowman Co.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from The Rupp & Bowman Co. in the registry?

The most recently registered devices listed for The Rupp & Bowman Co. include KONE CALCIUM TEST, SPECIFIC CHEMISTRY ANALYZER and MICROLYTE 7.

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