Carestream gets FDA nod for CR mammo

Carestream Health has received an approval letter from the FDA for its computed radiography (CR) system for mammography.

The company said its Carestream DirectView CR Mammography Feature enables mammography images to be captured digitally while utilizing a healthcare provider’s existing mammography x-ray unit and workflow processes. It is intended for use in the same clinical applications as traditional screen-film based mammography systems.

This optional mammography feature is available when purchasing a new Carestream DirectView Elite, Classic or CR 975 System, or as a retrofit to installed Elite, Classic or CR 850/950/975 systems.

With this feature, Carestream’s CR systems can be used for both general radiography and mammography exams. In addition, the optional Carestream DirectView CR Mammography Total Quality Tool is available to streamline objective mammography image testing and QC measurements, according to the Rochester, N.Y.-based company

Carestream has sold its CR mammography feature in Europe, Greater Asia, Japan and Latin America since 2005 and installed systems with its mammography capability in clinics, breast imaging centers and hospitals. In addition, Carestream has sold the system in Canada since 2007 after it received regulatory approval from Health Canada.

Once the FDA approves the final product labeling, Carestream said it will begin distribution in the U.S.


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