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U.S. Department of Health and Human Services

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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FDA Recall
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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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