FDA Approves Canon’s Compressed SPEEDER Software for MRI
Canon Medical Systems announced that the U.S. Food & Drug Administration (FDA) has cleared its Compressed SPEEDER technology for use in the company’s Vantage Orian 1.5T MRI system.
Canon Medical Systems announced that the U.S. Food & Drug Administration (FDA) has cleared its Compressed SPEEDER technology for use in the company’s Vantage Orian 1.5T MRI system.
The technology, which is also available on the Vantage Galan 3T MRI system, can help reduce overall MRI scan times by reconstructing full resolution images from under-sampled data and avoiding unfolding error artifacts. In addition, it can help capture higher resolution images in 2D Fast Spin Echo acquisitions.
Reduced scan time not only presents an advantage for patients who find it difficult to remain still during long scans, but it also allows for additional time for disinfection of MRI systems and imaging suites between patients as practices begin to return to more normal patient volumes.
Faced with new, stringent cleaning protocols, more complex patient appointment management and other changes to workflow, the Compressed SPEEDER technology may help ease some post-pandemic growing pains for radiology departments and practices as many work to adjust to the “new normal.”
Canon’s new technology is included in an updated version of the M-Power software available for the Vantage Orian 1.5T. The software comes standard with Windows 10 and cybersecurity functionality, including continuous updates from Microsoft and whitelisting functions which allow for access only to authorized applications and processes.
“In MR imaging, shortening scan times is vastly important for both the patient and physician,” said Jonathan Furuyama, managing director, MR Business Unit, Canon Medical Systems USA, Inc., in a statement. “With the help of Compressed SPEEDER along with Windows 10 on the Vantage Orian 1.5T MR system, healthcare providers can offer a quick, comfortable and safe experience for their patients.”
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