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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 26 of 26 Results
510(K) Number: K010721
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FDA Recall
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Axiom Artis X-Ray System using software version VB11D or VB20B 2 05/03/2005 Siemens Medical Solutions USA, Inc
Axiom Artis BA or BC Biplane System, Angiographic x-ray system, Model number 59 04 649 2 09/14/2004 Siemens Medical Solutions USA, Inc
Axiom Artis BA or BC Biplane System, Angiographic x-ray system, Model number 59 04 656 2 09/14/2004 Siemens Medical Solutions USA, Inc
SIEMENS AXIOM Artis - AUTOMAP FUNCTION 2 07/20/2004 Siemens Medical Solutions USA, Inc
Axiom Artis System 2 07/20/2004 Siemens Medical Solutions USA, Inc
Axiom Artis System, X-ray, Angiographic 2 12/18/2002 Siemens Medical Systems Inc
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