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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 114 Results
510(K) Number: K080107
 
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Product Description
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VITEK 2 Gram Negative Susceptibility Card, AST-N184, REF 411 154, For In Vitro Diagnostic Use, 20 ca... 1 04/27/2011 FEI # 1950204
Biomerieux Inc
VITEK 2 Gram Negative Susceptibility Card, AST-N183, REF 411 021, For In Vitro Diagnostic Use, 20 ca... 1 04/27/2011 FEI # 1950204
Biomerieux Inc
VITEK 2 Gram Negative Susceptibility Card, AST-N182, REF 410 804, For In Vitro Diagnostic Use, 20 c... 1 11/11/2010 FEI # 1950204
Biomerieux Inc
VITEK 2 Gram Negative Susceptibility Card, AST-N181, REF 410 803, For In Vitro Diagnostic Use, 20 c... 1 11/11/2010 FEI # 1950204
Biomerieux Inc
VITEK 2 Gram Negative Susceptibility Card, AST-N180, REF 410 771, For In Vitro Diagnostic Use, 20 c... 1 11/11/2010 FEI # 1950204
Biomerieux Inc
VITEK 2 Gram Negative Susceptibility Card, AST-N179, REF 410 640, For In Vitro Diagnostic Use, 20 c... 1 11/11/2010 FEI # 1950204
Biomerieux Inc
VITEK 2 Gram Negative Susceptibility Card, AST-N178, REF 410 393, For In Vitro Diagnostic Use, 20 c... 1 11/11/2010 FEI # 1950204
Biomerieux Inc
VITEK 2 Gram Negative Susceptibility Card, AST-N177, REF 410 392, For In Vitro Diagnostic Use, 20 c... 1 11/11/2010 FEI # 1950204
Biomerieux Inc
VITEK 2 Gram Negative Susceptibility Card, AST-N176, REF 410 402, For In Vitro Diagnostic Use, 20 c... 1 11/11/2010 FEI # 1950204
Biomerieux Inc
VITEK 2 Gram Negative Susceptibility Card, AST-N175, REF 410 403, For In Vitro Diagnostic Use, 20 c... 1 11/11/2010 FEI # 1950204
Biomerieux Inc
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