Guidewires

Kendall

by EV3, Inc

A sterile hand-operated device intended to be attached to the proximal end of an invasive device (e.g., a catheter, a needle, or a guidewire) to provide the operator with the ability to manually manipulate and control the directional torque (rotation) of the device to which it is attached. This device may be made of plastic or metal materials. This is a single-use device.

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Kendall models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
WWTD35001— Not statedAvailable

FDA clearances

  • 510(k) K120863 April 2012

Procedures that use guidewires

Frequently asked questions

What is Kendall used for?

A sterile hand-operated device intended to be attached to the proximal end of an invasive device (e.g., a catheter, a needle, or a guidewire) to provide the operator with the ability to manually manipulate and control the directional torque (rotation) of the device to which it is attached. This device may be made of plastic or metal materials. This is a single-use device.

Who makes Kendall?

Kendall is made by EV3, Inc. It is listed under guidewires in our device library.

What sizes does Kendall come in?

The FDA device database does not list sizes for Kendall. Check the instructions for use or ask a EV3, Inc representative.

Is Kendall MRI safe?

The FDA device database entry for Kendall does not state its MRI safety status. Check the labeling before MRI.

Is Kendall FDA cleared?

Kendall is covered by FDA submission K120863.

How do I contact a EV3, Inc sales representative?

EV3, Inc has not listed representatives on LA Vascular yet. Visit the EV3, Inc company page for contact details.

Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.

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