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