Medical Device Recalls
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1 result found
510(K) Number: K110366 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| syngo.via syngo.CT Cardiac Function, Model Number 10496180 Product Usage: Syngo.CT Cardiac Plann... | 2 | 04/09/2019 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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