Medical Device Recalls
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1 result found
510(K) Number: K101036 |
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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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| R-20J , Diagnostic X-Ray Beam-Limiting Device. In combination with any of below X-Ray tubes: 06... | 2 | 11/08/2012 |
FEI # 1000125362 Shimadzu Medical Systems |
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