Medical Device Recalls
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1 result found
510(K) Number: K202394 |
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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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The EOSedge system may acquire two simultaneous orthogonal planar images for a standing or seated pa... | 2 | 04/13/2021 | EOS Imaging |
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