Source-Ray, Inc. Receives FDA 510(k) Approval For The Model SR-130-D Digital Portable X-Ray System

BOHEMIA, N.Y. – December 13, 2004

Source-Ray, Inc. announced today that it has received its 510(k) approval from the Food & Drug Administration for its model SR-130-D Direct Capture Digital Portable X-Ray System and will ramp–up production for March 05 product availability.

The SR-130-D utilizes the Canon Medical Systems CXDI-50G Large Format 14" x 17" direct capture digital x-ray sensor panel.  The SR-130-D provides anatomical programming and patient data storage.  The x-ray technician can capture and preview the image for anatomical accuracy, store the image or electronically send the image to an off-site radiologist for clinical diagnosis. The SR-130-D reduces exam time - each image is captured, verified and clinically reviewed in seconds by the x-ray technician. Technique-based retakes are virtually eliminated.  Patient movement-based retakes can be performed immediately, while the patient is still in position.  Because the SR-130-D delivers superior diagnostic content and image processing capabilities, patient care is enhanced.  The system’s inherent high resolution and wide exposure latitude produces consistent, detailed diagnostic content.  Image processing capabilities allow images to be enhanced for better visualization.

The SR-130-D makes financial sense in many clinical applications by eliminating the recurring cost of film, chemicals, chemical disposal, cassettes, and processor maintenance. The SR-130-D can reduce the amount of time and labor it takes to produce and manage images, eliminate technique-based retakes, and cost savings can begin immediately.  

The SR-130-D will provide faster results, better diagnostics, deliver more efficient and cost effective clinical performance.

The SR-130-D is DICOM 3 compatible.

Dealer inquires welcomed

Contact:  Jerry Palmese, Director of Sales & Marketing

                (631) 244-8200, (631) 244-7464 (fax)