Medical Device Recalls
-
1 result found
510(K) Number: K110637 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
OneTouch Verio IQ Blood Glucose Monitoring System Kit; One Touch Verio IQ Blood Glucose IQ Blood Gl... | 2 | 04/02/2012 | Lifescan Inc |
-