Medical Device Recalls
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1 result found
510(K) Number: K143029 |
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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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| The GC80 Digital X-ray Imaging System | 2 | 03/02/2018 |
FEI # 3004938766 NeuroLogica Corporation |
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