Medical Device Recalls
-
|
1 result found
510(K) Number: K911056 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| siemens Dimension® Phenytoin Flex® Reagent Cartridge The PTN method used on the Dimension® clinic... | 2 | 10/29/2014 | Siemens Healthcare Diagnostics, Inc. |
-







