Medical Device Recalls
-
|
1 result found
510(K) Number: K101203 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| COBAS INTEGRA 400 plus analyzer used in the following assays: a)Tina-quant Apolipoprotein A-1 ver.2... | 2 | 04/10/2019 | Roche Diagnostics Corporation |
-







