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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K213516
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Upgrade to MR 7700. Product Code (REF): 782130. MR systems with SW version R11.1 and R12.1. 2 01/29/2026 FEI # 3006648320
Philips North America
MR 7700. Product Code (REF): (1) 782120, (2) 782153. MR systems with SW version R11.1 and R12.1.... 2 01/29/2026 FEI # 3006648320
Philips North America
MR 7700 Model Numbers (REF): (1) 782120, (2) 782153; 2 07/30/2025 FEI # 3006648320
Philips North America
Product Name: Upgrade to MR 7700; Model Number: 782130; 2 05/16/2025 FEI # 3016618143
Philips North America Llc
Product Name: MR 7700; Model Numbers: (1) 782120, (2) 782153; 2 05/16/2025 FEI # 3016618143
Philips North America Llc
MR 7700, Magnetic Resonance System. 2 04/17/2024 FEI # 3016618143
Philips North America Llc
Ingenia 3.0T CX. Model (REF) Numbers 781271, 782105. 2 02/01/2024 FEI # 3006648320
Philips North America
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