Medical Device Recalls
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1 result found
510(K) Number: K850397 |
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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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| Integrated Orbiter Single Detector General Purpose Gamma Camera System; Siemens Medical Systems, Inc... | 2 | 03/06/2003 |
FEI # 1000514697 Siemens Medical Solutions USA, Inc. |
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