Medical Device Recalls
-
|
1 result found
510(K) Number: K031380 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Beckman Coulter HbA1c APT (Hemoglobin A1c, Whole Blood Application), Part Number: OSR61177, Lot Numb... | 2 | 05/10/2011 |
FEI # 2050012 Beckman Coulter Inc. |
-







