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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K213516
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FDA Recall
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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
Philips Upgrade to MR 7700 System, Model Number 782130 2 12/08/2022 Philips North America Llc
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