Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K011900 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Glucose Hexokinase (Liquid) Reagent For the in vitro quantitative determination of Glucose in ser... | 2 | 12/18/2014 |
FEI # 3003071743 JAS Diagnostics Inc. |
| Glucose Hexokinase Liquid Reagent For the in vitro quantitative determination of Glucose in serum. ... | 2 | 06/25/2014 |
FEI # 3003071743 JAS Diagnostics Inc. |
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