Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K133910 |
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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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nordicBrainEX, software versions 2.21 through 2.3.10 | 2 | 07/25/2022 | NordicNeuroLab AS |
nordicBrainEx 2.0 provides analysis and visualization capabilities of dynamic MRI data of the brain,... | 2 | 06/01/2018 | NordicNeuroLab AS |
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