Medical Device Recalls
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21 to 21 of 21 Results
510(K) Number: K021021 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Mavig Portegra 2 which is an accessory to the Siemens angiographic, fluoroscopic and radiographic im... | 2 | 06/16/2009 | Siemens Medical Solutions USA, Inc |
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