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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
510(K) Number: K013858
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FDA Recall
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Philips MR Systems: Asset 0.5T, Apollo 0.5T, Infinion 1.5T, Eclipse/Polaris 1.5T, Panorama 0.6T ... 2 10/21/2013 Philips Medical Systems (Cleveland) Inc
Panorama 0.6T MRI Nuclear Magnetic Resonance Imaging System, Philips Panorama 0.6T Open MRI system, ... 2 09/17/2010 Philips Medical Systems North America Co. Phillips
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