Medical Device Recalls
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1 result found
510(K) Number: K133782 |
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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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| Sedecal NOVA FA DR System. for diagnostic radiography. | 2 | 11/20/2018 |
FEI # 3002495042 Sedecal S.A. |
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