Medical Device Recalls
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1 to 10 of 26 Results
510(K) Number: K010721 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Axiom Artis System, X-ray, Angiographic | 2 | 12/18/2002 | Siemens Medical Systems Inc |
Axiom Artis System | 2 | 07/20/2004 | Siemens Medical Solutions USA, Inc |
SIEMENS AXIOM Artis - AUTOMAP FUNCTION | 2 | 07/20/2004 | 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 |
Axiom Artis X-Ray System using software version VB11D or VB20B | 2 | 05/03/2005 | Siemens Medical Solutions USA, Inc |
Axiom Artis MP X-Ray System | 2 | 05/11/2005 | Siemens Medical Solutions USA, Inc |
AXIOM Artis MP, Angiographic x-ray system, model number 5904466 | 2 | 03/08/2007 | Siemens Medical Solutions USA, Inc |
AXIOM Artis MP, Angiographic x-ray system, model number 7555365 | 2 | 03/08/2007 | Siemens Medical Solutions USA, Inc |
AXIOM Artis. Angiographic X-ray System. | 2 | 11/04/2008 | Siemens Medical Solutions USA, Inc |
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