Medical Device Recalls
-
|
1 result found
510(K) Number: K061020 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Dimension Vista Aspartate Aminotransferase (AST) assay; (Product Number: K2014/10445148) (Mfr: Sieme... | 2 | 05/04/2018 | Siemens Healthcare Diagnostics, Inc. |
-







