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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K913687
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Cholestech LDX Multi-Analyte Controls, Level 1 & 2, 1 vial set, Catalog Number 12-712. Assayed qu... 2 11/22/2010 Biosite Inc Dba Innovacon Inc.
Cholestech LDX Multi-Analyte Controls, Level 1 & 2, 3 vial set, Catalog Number 12-713. Assayed qu... 2 11/22/2010 Biosite Inc Dba Innovacon Inc.
Cholestech LDX Calibration Verification, Levels 1-4, Catalog Number 11-255. To be used for verify... 2 11/22/2010 Biosite Inc Dba Innovacon Inc.
Cholestech LDX Lipid Controls, Level 1 & 2, 3 vial set, Catalog Number 10-983. Assayed quality co... 2 11/22/2010 Biosite Inc Dba Innovacon Inc.
Cholestech LDX Lipid Controls, Level 1 & 2, 1 vial set, Catalog Number 10-982. Assayed quality co... 2 11/22/2010 Biosite Inc Dba Innovacon Inc.
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