Medical Device Recalls
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1 result found
510(K) Number: K945293 |
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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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ACOM.M angiographic x ray system. Model number 4371741 | 2 | 09/18/2004 | Siemens Medical Solutions USA, Inc |
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