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U.S. Department of Health and Human Services

510(k) Premarket Notification
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21 to 30 of 41 Results
ProductCode: JAA Applicant: SIEMENS MEDICAL SOLUTIONS USA, INC Decision Date To: 01/21/2017
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artis one SIEMENS MEDICAL SOLUTIONS USA, INC. K133580 04/28/2014
artis q and q.zen- modular angiographic system SIEMENS MEDICAL SOLUTIONS USA, INC. K123529 02/26/2013
syngo aortic valveguide software SIEMENS MEDICAL SOLUTIONS USA, INC. K113027 11/22/2011
luminos agile SIEMENS MEDICAL SOLUTIONS USA, INC. K111292 06/03/2011
uroskop omnia SIEMENS MEDICAL SOLUTIONS USA, INC. K101491 06/30/2010
axiom luminos drf SIEMENS MEDICAL SOLUTIONS USA, INC. K062623 08/22/2007
axiom artis - modular angiographic system SIEMENS MEDICAL SOLUTIONS USA, INC. K052202 03/07/2006
siremobile c06 SIEMENS MEDICAL SOLUTIONS USA, INC. K040066 02/12/2004
modular angiography system axiom artis SIEMENS MEDICAL SOLUTIONS USA, INC. K021021 06/06/2002
u04 SIEMENS MEDICAL SOLUTIONS USA, INC. K010942 04/12/2001
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