Medical Device Recalls
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1 result found
510(K) Number: K092253 |
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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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fMRI Hardware System VisualSystem allows video signals from the stimulus presentation PC to enter ... | 2 | 09/11/2018 | NordicNeuroLab AS |
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