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Fujifilm's Aspire HD Receives FDA Clearance
Date:9/12/2011

STAMFORD, Conn., Sept. 12, 2011 /PRNewswire/ -- Breast Imaging facilities looking for increased diagnostic confidence in mammography screening can now benefit from the exceptional image quality of the Aspire™ HD Full Field Digital Mammography (FFDM) system from FUJIFILM Medical Systems U.S.A., Inc. Now FDA 510(k) cleared, the Aspire HD provides image clarity that enables extraordinary detail of potential abnormalities that not only assists in more accurate and reliable diagnoses, but also results in enhanced clinician productivity.

(Photo:  http://photos.prnewswire.com/prnh/20110316/NY65935)

The exceptional image quality of the Aspire HD is made possible in part by the system's unique proprietary detector that uses innovative dual layer amorphous selenium (a-Se) and the first use of Fujifilm's innovative Direct Optical Switching (DOS) technology. This new technology combined with the company's renowned 50-micron resolution provides facilities with the confidence they need for the detailed visualization that's required in mammography.

"Breast imaging facilities and their patients deserve the latest and most reliable technologies," says David Hotchkiss, Director, Product Marketing, Modality Solutions for Fujifilm. "As we build upon our proven technological foundation for mammography, Fujifilm will continue to provide exceptional image quality that will raise the bar for performance and reliability in breast screening."

The new DOS technology eliminates the use of Thin Film Transistors (TFTs) which are currently used in typical FFDM detector systems. By eliminating the TFTs, this new technology creates a direct image transfer that results in a higher efficiency image capture.  This process produces images with less noise and the potential to reduce dose, while delivering the performance and reliability digital mammography users have come to expect fr
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SOURCE FUJIFILM Medical Systems U.S.A., Inc.
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