Medical Device Recalls
-
1 result found
510(K) Number: K974733 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
LDL-Cholesterol plus gen.2. The Boehringer Mannheim Direct LDL-Cholesterol test in intended for ... | 2 | 06/27/2015 | Roche Diagnostics Operations, Inc. |
-