Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K992660 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Iconos R200 C20, Iconos R200 T20, Iconos R100, Iconos MD, Iconos RHD, Luminos RF Classic, Luminos Fu... | 2 | 04/11/2013 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Axiom Iconos R200 X-Ray | 2 | 03/27/2010 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| Mavig Portegra 2 which is an accessory to the Siemens angiographic, fluoroscopic and radiographic im... | 2 | 06/16/2009 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
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