Medical Device Recalls
-
|
1 result found
510(K) Number: K080887 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| The UF-1000i is a fully automated urine particle analyzer intended for vitro diagnostic use in urina... | 2 | 02/10/2014 |
FEI # 1000515253 Sysmex America, Inc. |
-







