Medical Device Recalls
-
|
11 to 11 of 11 Results
510(K) Number: K060256 |
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| UniCel DxC 600i, Part Numbers: A25638, A25639, Beckman Coulter, Inc. | 2 | 05/24/2008 |
FEI # 2050012 Beckman Coulter Inc |
-







