CHICAGO, November 28, 2011 /PRNewswire/ — Royal Philips Electronics (NYSE: PHG, AEX: PHI) is announcing 510(k) clearance from the Food and Drug Administration (FDA) for the company’s first commercially available whole body positron emission tomography/magnetic resonance (PET/MR) imaging system, the Ingenuity TF PET/MR. This leading edge platform will redefine how medicine is practiced in the future by helping clinicians and researchers investigate novel personalized medicine and treatments for oncology, cardiology and neurology. The system is on display at the 97th annual meeting of the Radiological Society of North America (RSNA), November 27 – December 2…..

http://www.multivu.com/mnr/53109-philips-fda-clearance-market-whole-body-pet-mr-imaging-system