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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K183063
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SmartPath to dStream for XR and 3.0T. Product Code (REF): 781270. MR systems with SW version R11... 2 01/29/2026 FEI # 3006648320
Philips North America
Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781260.... 2 04/27/2026 FEI # 3006648320
Philips North America
Philips Ingenia 1.5T CX with MR Elastography (MRE). 1. Model Number (REF): 781262. 2 04/27/2026 FEI # 3006648320
Philips North America
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