Biopsy needles

DualCore Biopsy System-14g x 10cm

by Izi Medical Products, LLC

A collection of sterile devices designed to perform a non-specific soft tissue biopsy. It includes the biopsy needle used for this procedure; it does not include a pharmaceutical. This is a single-use device.

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DualCore Biopsy System-14g x 10cm models and sizes

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

Model / catalog no.SizeMRIStatus
MCN1210Length 10 cm Not statedAvailable
MCN1216Length 16 cm Not statedAvailable
MCN1410Length 10 cm Not statedAvailable
MCN1416Length 16 cm Not statedAvailable
MCN1610Length 10 cm Not statedAvailable
MCN1616Length 16 cm Not statedAvailable

FDA clearances

  • 510(k) K973565 November 1997

Procedures that use biopsy needles

Frequently asked questions

What is DualCore Biopsy System-14g x 10cm used for?

A collection of sterile devices designed to perform a non-specific soft tissue biopsy. It includes the biopsy needle used for this procedure; it does not include a pharmaceutical. This is a single-use device.

Who makes DualCore Biopsy System-14g x 10cm?

DualCore Biopsy System-14g x 10cm is made by Izi Medical Products, LLC. It is listed under biopsy needles and systems in our device library.

What sizes does DualCore Biopsy System-14g x 10cm come in?

Sizes listed for DualCore Biopsy System-14g x 10cm: Length: 10–16 cm. Confirm availability with the manufacturer's instructions for use.

Is DualCore Biopsy System-14g x 10cm MRI safe?

The FDA device database entry for DualCore Biopsy System-14g x 10cm does not state its MRI safety status. Check the labeling before MRI.

Is DualCore Biopsy System-14g x 10cm FDA cleared?

DualCore Biopsy System-14g x 10cm is covered by FDA submission K973565.

How do I contact a Izi Medical Products, LLC sales representative?

Izi Medical Products, LLC has not listed representatives on LA Vascular yet. Visit the Izi Medical Products, LLC 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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