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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 9 of 9 Results
510(K) Number: K945915
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Roche brand OMNI 9 Analyzer; catalog numbers GD0475, GD0475R and GD047591. 2 07/20/2004 FEI # 1823260
Roche Diagnostics Corp.
Roche brand OMNI 8 Analyzer; catalog numbers GD0455 and GD0455R. 2 07/20/2004 FEI # 1823260
Roche Diagnostics Corp.
Roche brand OMNI 7 Analyzer; catalog numbers GD0435 and GD0435R. 2 07/20/2004 FEI # 1823260
Roche Diagnostics Corp.
Roche brand OMNI 6 Analyzer; catalog numbers GD0415, GD0415R and GD041591. 2 07/20/2004 FEI # 1823260
Roche Diagnostics Corp.
Roche brand OMNI 5 Analyzer; catalog numbers GD0395 and GD0395R. 2 07/20/2004 FEI # 1823260
Roche Diagnostics Corp.
Roche brand OMNI 4 Analyzer; catalog numbers GD0375 and GD0375R . 2 07/20/2004 FEI # 1823260
Roche Diagnostics Corp.
Roche brand OMNI 3 Analyzer; catalog numbers GD0355, GD0355R and GD035591. 2 07/20/2004 FEI # 1823260
Roche Diagnostics Corp.
Roche brand OMNI 2 Analyzer; catalog numbers GD0335 and GD0335R. 2 07/20/2004 FEI # 1823260
Roche Diagnostics Corp.
Roche brand OMNI 1 Analyzer; catalog numbers GD0315 and GD0315R. 2 07/20/2004 FEI # 1823260
Roche Diagnostics Corp.
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