Medical Device Recalls
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21 to 26 of 26 Results
510(K) Number: K010721 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
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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