Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K060854 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ABX PENTRA Triglycerides CP ref. A11A01640 is an in vitro diagnostic assay for the quantitative dete... | 2 | 02/02/2016 | Horiba Instruments Inc |
The ABX PENTRA Cholesterol CP ref. A11A01634 is an in vitro diagnostic assay for quantitative determ... | 2 | 02/02/2016 | Horiba Instruments Inc |
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