Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K020232 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Hypoguard Advance Blood Glucose Strips, 10, 50, and 100 strip bottles. | 2 | 12/25/2003 |
FEI # 1832816 Hypoguard USA, Inc. |
| Hypoguard Advance Blood Glucose Monitoring System, includes Hypoguard Advance Blood Glucose Meter an... | 2 | 12/25/2003 |
FEI # 1832816 Hypoguard USA, Inc. |
-







