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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 17 Results
510(K) Number: K212673
 
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SmartPath to dStream for XR and 3.0T- For use as a diagnostic device to obtain cross-sectional imag... 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
Product Name: MR 5300; Model Numbers: (1) 782110, (2) 782152; 2 05/16/2025 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- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diag... 2 05/17/2024 Philips North America Llc
MR 5300, Magnetic Resonance System. 2 04/17/2024 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
MR 5300 Model Numbers (REF): (1) 782110, (2) 782135 (China ONLY), (3) 782152; 2 07/30/2025 Philips North America
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
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