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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 13 Results
510(K) Number: K213516
 
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Ingenia Elition X, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
Ingenia Elition S, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
MR 7700, Magnetic Resonance System. 2 04/17/2024 Philips North America Llc
Ingenia 3.0T CX, Model (REF) Numbers 781271, 782105 2 02/01/2024 Philips North America
Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106 2 08/11/2023 Philips North America
Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartP... 2 08/11/2023 Philips North America
Ingenia Elition X Magnetic Resonance (MR) system, Product Numbers 781358, 782107, and 782118 (SmartP... 2 08/11/2023 Philips North America
Ingenia Elition S Magnetic Resonance (MR) system, Product Numbers 781357 and 782106 2 08/11/2023 Philips North America
Philips MR 7700 System, Model Number 782120 2 12/08/2022 Philips North America Llc
Philips SmartPath to Ingenia Elition X MR System, Model Numbers 782118, 782132, 782144 2 12/08/2022 Philips North America Llc
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