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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K933588
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Product Description
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APhL® HRP IgG & IgM ELISA Kit; Ref. #LAPL-K-HRP-00GM; in vitro diagnostic. Distributed by Louisvill... 3 10/04/2007 Louisville Apl Diagnostics Inc
APhL® HRP IgG & IgM ELISA Kit; Ref. #LAPL-K-HRP-00GM; distributed by Louisville APL Diagnostics, Inc... 2 08/17/2007 Louisville Apl Diagnostics Inc
APhL® HRP IgM ELISA Kit; Ref. #LAPL-K-HRP-001M; distributed by Louisville APL Diagnostics, Inc., Dor... 2 08/17/2007 Louisville Apl Diagnostics Inc
APhL® HRP IgG ELISA Kit; Ref. #LAPL-K-HRP-001G; distributed by Louisville APL Diagnostics, Inc., Dor... 2 08/17/2007 Louisville Apl Diagnostics Inc
american diagnostica inc. IgM Conjugate, 15mL; component of the american diagnostica, inc. IMUCLONE®... 2 07/24/2007 Louisville Apl Diagnostics Inc
american diagnostica inc. IgG Conjugate, 15mL; component of the american diagnostica, inc. IMUCLONE®... 2 07/24/2007 Louisville Apl Diagnostics Inc
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