Medical Device Recalls
-
|
1 result found
510(K) Number: K922704 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| COULTER MAXM Hematology Analyzer/MAXM Hematology Analyzer with Autoloader Part number: 6705995, 67... | 2 | 01/11/2012 |
FEI # 2050012 Beckman Coulter Inc. |
-







