Medical Device Recalls
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1 result found
510(K) Number: K123306 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| nordicTumorEx 1.0 nordicTumorEx is an image processing software package to be used by trained p... | 2 | 05/31/2018 |
FEI # 3006738448 NordicNeuroLab AS |
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