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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 28 Results
510(K) Number: K052202
 
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AXIOM Artis BA, Model Number 5904656 2 07/22/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
AXIOM Artis BC, Model Number 5904649 2 07/22/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
AXIOM Artis FA, Model Number 5904441 2 07/22/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
AXIOM Artis FC, Model Number 5904433 2 07/22/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
AXIOM Artis MP, Model Number 5904466 2 07/22/2019 FEI # 2240869
Siemens Medical Solutions USA, Inc
AXIOM Artis System dBA using software version VB31D with 30x40 cm2 flat detectors. ®AXIOM Artis i... 2 12/09/2008 FEI # 2240869
Siemens Medical Solutions USA, Inc
AXIOM Artis System dFA using software version VB31D with 30x40 cm2 flat detectors. ®AXIOM Artis i... 2 12/09/2008 FEI # 2240869
Siemens Medical Solutions USA, Inc
AXIOM Artis System dFC using software version VB31D with 30x40 cm2 flat detectors. ®AXIOM Artis i... 2 12/09/2008 FEI # 2240869
Siemens Medical Solutions USA, Inc
AXIOM Artis System dMP using software version VB31D with 30x40 cm2 flat detectors. ®AXIOM Artis i... 2 12/09/2008 FEI # 2240869
Siemens Medical Solutions USA, Inc
AXIOM Artis System dTA using software version VB31D with 30x40 cm2 flat detectors. ®AXIOM Artis i... 2 12/09/2008 FEI # 2240869
Siemens Medical Solutions USA, Inc
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