Breast: Page 342

IDSI submits 510(k) for CTLM
By AuntMinnie.com staff writers
Imaging Diagnostic Systems (IDSI) this week submitted a 510(k) premarket notification to the U.S. Food and Drug Administration for its CT laser mammography (CTLM) breast imaging device.
November 22, 2010
Hologic's Selenia nets FDA letter
By AuntMinnie.com staff writers
Women's healthcare vendor Hologic has received an approvable letter from the U.S. Food and Drug Administration for the Selenia Dimensions 3D digital mammography tomosynthesis system.
November 22, 2010
Mammotome gets FDA nod
By AuntMinnie.com staff writers
Breast biopsy developer Mammotome has received U.S. Food and Drug Administration 510(k) clearance for its Mammotome Molecular Imaging (MI) system.
November 22, 2010
Vidar unveils new ClinicalExpress
By AuntMinnie.com staff writers
Film digitizer vendor Vidar Systems will release version 5.0 of its ClinicalExpress DICOM acquisition software for general radiography and mammography at the RSNA meeting in Chicago.
November 22, 2010
Targeted breast US best for women under 30
By AuntMinnie.com staff writers
Targeted breast ultrasound is the best way to evaluate focal breast signs and symptoms of disease in women younger than 30, according to a new study in the December issue of the American Journal of Roentgenology.
November 21, 2010
Mammo screening reduces death rate in medium-risk women
By Kate Madden Yee
Yearly mammography in women in their 40s with a medium familial risk of breast cancer can reduce the mortality rate by almost 30%, according to new research published online November 18 in Lancet.
November 18, 2010
Ga. RT enters not guilty plea
By AuntMinnie.com staff writers
A radiologic technologist (RT) in Georgia accused of submitting false mammogram results entered a plea of not guilty in a hearing on November 17.
November 18, 2010
Preoperative MRI predicts upgrade of DCIS to invasive breast cancer
By Eric Barnes
Tuesday, November 30 | 3:50 p.m.-4:00 p.m. | SSJ01-06 | Room E352MRI of ductal carcinoma in situ (DCIS) can help determine which lesions are likely to upgrade to invasive cancers, researchers from New York University Medical Center in New York City will report in this Tuesday afternoon presentation.
November 18, 2010
Breast biopsies successful with integrated 3D digital breast tomosynthesis
By Eric Barnes
Tuesday, November 30 | 3:00 p.m.-3:10 p.m.| SSJ01-01 | Room E352French researchers using 3D digital breast tomosynthesis are finding lesions that can't be visualized on conventional 2D mammography, and by integrating a tomosynthesis biopsy unit, they say they can biopsy and analyze a broader range of breast lesions compared with 2D digital mammography.
November 18, 2010
FDA clears Volpara breast density software
By AuntMinnie.com staff writers
The U.S. Food and Drug Administration has cleared the Volpara breast density software from Volpara, Ltd., a subsidiary of Matakina Technology.
November 17, 2010
FDA's revision of FFDM rules may break market logjam
By James Brice
Breast imaging providers in the U.S. may soon witness a surge of new full-field digital mammography (FFDM) products on the market, thanks to the U.S. Food and Drug Administration's November 4 decision to ease its rules for approval of FFDM technology.
November 17, 2010
DISC launches QA Mamchex for Carestream
By AuntMinnie.com staff writers
Radiography quality control technology developer Diagnostic Imaging Specialists (DISC) has launched its DISC QA Mamchex tool for use with Carestream Health's DirectView computed radiography mammography system.
November 17, 2010
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