Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K163116 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Ingenia 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic devic... | 2 | 09/03/2021 | Philips North America Llc |
Ingenia 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device... | 2 | 08/25/2021 | Philips North America Llc |
Ingenia 1.5T-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device... | 2 | 08/25/2021 | Philips North America Llc |
Ingenia 3.0T, Model Number 781377. Nuclear Magnetic Resonance Imaging System | 2 | 02/22/2019 | Philips Medical Systems Nederlands |
Ingenia 1.5T, Model Number 781341. Nuclear Magnetic Resonance Imaging System | 2 | 02/22/2019 | Philips Medical Systems Nederlands |
Ingenia 1.5T, Model Number 781396. Nuclear Magnetic Resonance Imaging System | 2 | 02/22/2019 | Philips Medical Systems Nederlands |
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