Medical Device Recalls
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1 result found
510(K) Number: K002137 |
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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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Cathcor/LX/Desktop, System, X-Ray, Angiographic | 3 | 07/19/2003 | Siemens Medical Solutions USA, Inc |
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