Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K173451 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Ingenia Elition S-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic ... | 2 | 09/03/2021 | Philips North America Llc |
Ingenia Elition X-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic ... | 2 | 09/03/2021 | Philips North America Llc |
Ingenia Elition S-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic d... | 2 | 08/25/2021 | Philips North America Llc |
Ingenia Elition X-Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic d... | 2 | 08/25/2021 | Philips North America Llc |
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