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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 26 Results
510(K) Number: K213516
 
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Ingenia 1.5T -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images ... 2 09/20/2024 Philips North America Llc
Evolution Upgrade 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectrosco... 2 09/20/2024 Philips North America Llc
MR 7700 -For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/... 2 09/20/2024 Philips North America Llc
MR 5300 - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images and/... 2 09/20/2024 Philips North America Llc
Ingenia Elition X- For use as a diagnostic device to obtain cross-sectional images, spectroscopic im... 2 09/20/2024 Philips North America Llc
Ingenia Elition S -For use as a diagnostic device to obtain cross-sectional images, spectroscopic im... 2 09/20/2024 Philips North America Llc
SmartPath to Ingenia Elition X - For use as a diagnostic device to obtain cross-sectional images, sp... 2 09/20/2024 Philips North America Llc
Ingenia Ambition S - For use as a diagnostic device to obtain cross-sectional images, spectroscopic ... 2 09/20/2024 Philips North America Llc
Ingenia 3.0T CX - For use as a diagnostic device to obtain cross-sectional images, spectroscopic ima... 2 09/20/2024 Philips North America Llc
Ingenia 3.0T - For use as a diagnostic device to obtain cross-sectional images, spectroscopic images... 2 09/20/2024 Philips North America Llc
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