Philips receives FDA 510(k) clearance for latest breakthrough high-performance MR 7700 system
Koninklijke Philips N.V. NY Registry Shares (PHG)
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Source: GlobeNewswire
May 9, 2022 MR 7700 imaging system features an enhanced gradient system for unmatched performance and precision, delivering Philips’ highest image quality to help improve diagnostic outcomes Newest MR innovation from Philips integrates artificial intelligence [1] for improved workflow to enhance patient and staff experiencePhilips is the first to bring multi nuclei to clinical practice with seamless integration into standard user interface of 3.0T dStream systems Amsterdam, the Netherlands – Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, announced it has received FDA 510(k) clearance for the company’s new MR 7700 3.0T MR system. This latest break-through MR innovation from Philips delivers unmatched performance and precision for both research and advanced clinical diagnostics, helping to address the Quadruple Aim. The XP gradients of MR 7700 provide high accuracy to support a confident diagnosis for every patient with Philips’ highest quality diffus
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