Technology | March 18, 2009

FDA Clears Use of Bioptic’s Radiography System in Core Biopsy Analysis

March 18, 2009 – Bioptics Inc., which develops imaging technology for the detection and treatment of cancer, announced at the NCBC 2009 annual conference that the FDA has granted it 510(k) clearance to use the Core VISION, a specimen radiography system, to analyze Core Biopsy samples.

The Core VISION is small, simple to operate and has been ergonomically designed to speed the workflow during biopsy procedures and the results can be readily viewed by various clinicians through their standard PACS network and offers the highest resolution of any product in its class. The Core VISION is radiation shielded, interlocked and can be readily deployed in stereotactic procedure rooms.

“The Core VISION complements our range of specimen radiography products and greatly enhances workflow during core biopsy procedures at a very cost effective price,” said Market Development Manager Cheryl Augello.

For more information: www.bioptics-inc.com

Related Content

Oxipit Introduces Multilingual Support for ChestEye AI Imaging Suite
News | Artificial Intelligence | April 16, 2019
The CE-certified ChestEye artificial intelligence (AI) imaging suite by Oxipit is now available in seven European...
Check-Cap Initiates U.S. Pilot Study of C-Scan for Colorectal Cancer Screening
News | Colonoscopy Systems | April 15, 2019
Check-Cap Ltd. has initiated its U.S. pilot study of the C-Scan system for prevention of colorectal cancer through...
Enlitic Closes Series B Funding for Artificial Intelligence Solutions for Radiologists
News | Artificial Intelligence | April 08, 2019
Radiology artificial intelligence (AI) company Enlitic announced the close of its $15 million Series B financing round...
Videos | RSNA | April 03, 2019
ITN Editor Dave Fornell takes a tour of some of the most interesting new medical imaging technologies displa
News | Biopsy Systems | March 29, 2019
Dune Medical Devices has just completed the first in-man cases for Smart Biopsy, its percutaneous soft tissue biopsy...
Artificial Intelligence Can Improve Emergency X-ray Identification of Pacemakers
News | X-Ray | March 29, 2019
A research team from Imperial College London believes a new software could speed up the diagnosis and treatment of...
FDA Clears Mobilett Elara Max Mobile X-ray from Siemens Healthineers
Technology | Digital Radiography (DR) | March 20, 2019
The U.S. Food and Drug Administration (FDA) has cleared the Mobilett Elara Max mobile X-ray system from Siemens...
Shimadzu School of Radiologic Sciences Approved at Midwestern State University
News | Digital Radiography (DR) | March 05, 2019
Shimadzu Medical Systems USA (SMS) announced that The Shimadzu School of Radiologic Sciences has been approved by...
Agfa Receives FDA Clearance for DR 800 With Tomosynthesis
Technology | Digital Radiography (DR) | February 21, 2019
Agfa Healthcare has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its DR 800 multipurpose...
FDA Clears Ion Endoluminal Lung Biopsy System
Technology | Interventional Radiology | February 20, 2019
The U.S. Food and Drug Administration (FDA) cleared the Ion endoluminal system from Intuitive Surgical Inc. to enable...