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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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Brand Name: ® cobas c 6000 MODULAR Series System e 601 ® cobas c 8000 MODULAR Series System - e ... 2 01/16/2018 FEI # 1823260
Roche Diagnostics Corporation
Creatinine Plus. Intended for use on Hitachi/MODULAR systems for the quantitative determination o... 2 06/27/2015 FEI # 1823260
Roche Diagnostics Operations, Inc.
Modular E 170 Analyzer: Immunoassay Chemistry Analyzer, Chemistry (Photometric, Discrete) for clini... 2 03/28/2018 FEI # 1823260
Roche Diagnostics Corporation
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 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 MODULAR Analytics Combination Systems Modular D/P: Clinical Chemistry Analyzer, Chemi... 2 10/25/2016 FEI # 1823260
Roche Diagnostics Operations, Inc.
Roche/Hitachi Modular Additional D Module DAT clinical chemistry analyzer; catalog number 0442938916... 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 Analytical D Module clinical chemistry analyzer; catalog number 03739023001. 2 09/02/2004 FEI # 1823260
Roche Diagnostics Corp.
Roche/Hitachi Modular Analytics P clinical chemistry analyzer; Modular P. Catalog number 766-8156. 2 10/15/2003 FEI # 1823260
Roche Diagnostics Corp.
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