Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K082441 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| nordicICE v 2.3.14 nordicICE is an image processing software package to be used by trained profes... | 2 | 06/04/2018 | NordicNeuroLab AS |
| nordicICE 2.3.14 Image processing software package used by trained professionals, including phys... | 2 | 05/31/2018 | NordicNeuroLab AS |
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