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Keithley Development Co.

Country not established

Devices
2

What Keithley Development Co. makes

Keithley Development Co. manufactures the KEITHLEY CLAMP, a device used for securing or stabilizing medical components during procedures, and the KEITHLEY LYMPHOCYTE DEPLETION CART, a system designed for apheresis-based lymphocyte depletion therapies.

The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. The portfolio is listed in the FDA’s 510(k) clearance registry, and the manufacturer is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Keithley Clamp Ref K792256

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Keithley Lymphocyte Depletion Cart Ref K801899

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

Frequently asked questions

How many devices does Keithley Development Co. have in the registry?

The registry currently lists 2 devices for Keithley Development Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Keithley Development Co.'s devices?

Among its 2 most recently registered devices, Keithley Development Co. has devices listed in FDA 510(k) (2 devices).

What risk classes do Keithley Development Co.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Keithley Development Co.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Keithley Development Co. in the registry?

The most recently registered devices listed for Keithley Development Co. include KEITHLEY CLAMP and KEITHLEY LYMPHOCYTE DEPLETION CART.

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