Medical Device Recalls
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1 result found
510(K) Number: K130395 |
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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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steroEOS Workstation with software versions: 1.3, 1.4 and 1.5 used in processing 3D X-ray images ... | 2 | 12/26/2013 | EOS Imaging |
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