Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K110137 |
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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 Enzymatic Creatinine CP ref. A11A01907 reagent is intended for the quantitative in vitro ... | 2 | 02/02/2016 | Horiba Instruments Inc |
ABX PENTRA Urine Control L/H. The ABX PENTRA Urine Control L/H is a two-level (Low and High) qual... | 3 | 02/03/2014 | Horiba Instruments, Inc dba Horiba Medical |
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