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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 18 Results
510(K) Number: K953239
 
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Roche/Hitachi Modular Analytics P clinical chemistry analyzer; Modular P. Catalog number 766-8156. 2 10/15/2003 FEI # 1823260
Roche Diagnostics Corp.
Roche/Hitachi Modular Analytical D Module clinical chemistry analyzer; catalog number 03739023001. 2 09/02/2004 FEI # 1823260
Roche Diagnostics Corp.
Roche/Hitachi Modular Analytical D Module DAT clinical chemistry analyzer; catalog number 0442933816... 2 09/02/2004 FEI # 1823260
Roche Diagnostics Corp.
Roche/Hitachi Modular Additional D Module DAT clinical chemistry analyzer; catalog number 0442938916... 2 09/02/2004 FEI # 1823260
Roche Diagnostics Corp.
Roche/Hitachi K Electrode, a potassium electrode for use with the Roche/Hitachi models 717,747, 902,... 2 08/03/2006 FEI # 1823260
Roche Diagnostics Corp.
Roche/Hitachi K Electrode, a potassium electrode for use with the Roche/Hitachi models 717,747, 902,... 3 08/29/2006 FEI # 1823260
Roche Diagnostics Corp.
Roche/Hitachi Modular Analytics System, Modular P800 Module GMMI clinical chemistry analyzer; Catalo... 2 08/13/2008 FEI # 1823260
Roche Diagnostics Corp.
Roche/Hitachi Modular Analytics System, Modular D2400 Module GMMI clinical chemistry analyzer; Catal... 2 08/13/2008 FEI # 1823260
Roche Diagnostics Corp.
Roche/Hitachi Modular Analytics System, Modular D Module GMMI clinical chemistry analyzer; Catalog n... 2 08/13/2008 FEI # 1823260
Roche Diagnostics Corp.
Roche/Hitachi Modular Analytics System Modular P Module GMMI immunoassay analyzer; Catalog number 03... 2 08/13/2008 FEI # 1823260
Roche Diagnostics Corp.
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