Biopsy needles

Quick-Core Biopsy Qc-16-9.0-20t

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.

Contact a rep Compare similar devices

Quick-Core Biopsy Qc-16-9.0-20t models and sizes

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

Model / catalog no.SizeMRIStatus
G27007— Not statedAvailable

FDA clearances

  • 510(k) K973565 November 1997

Procedures that use biopsy needles

Frequently asked questions

What is Quick-Core Biopsy Qc-16-9.0-20t 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 Quick-Core Biopsy Qc-16-9.0-20t?

Quick-Core Biopsy Qc-16-9.0-20t is made by Izi Medical Products, LLC. It is listed under biopsy needles and systems in our device library.

What sizes does Quick-Core Biopsy Qc-16-9.0-20t come in?

The FDA device database does not list sizes for Quick-Core Biopsy Qc-16-9.0-20t. Check the instructions for use or ask a Izi Medical Products, LLC representative.

Is Quick-Core Biopsy Qc-16-9.0-20t MRI safe?

The FDA device database entry for Quick-Core Biopsy Qc-16-9.0-20t does not state its MRI safety status. Check the labeling before MRI.

Is Quick-Core Biopsy Qc-16-9.0-20t FDA cleared?

Quick-Core Biopsy Qc-16-9.0-20t 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.

📬 The IR Device Brief

One email a month: new FDA clearances, recalls and device pages in vascular & interventional radiology.

We'll email you a link to confirm. Unsubscribe any time.

Suggest edits

For manufacturers and their teams. Each field shows what the page says now: add, remove or rewrite anything, and leave the rest as is. LA Vascular reviews every change before it goes live.

About you