Medical Device Recalls
-
1 result found
510(K) Number: K051997 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Terumo Custom Cardiovascular Procedure Kit (manufactured to the design and specifications of the pu... | 2 | 05/11/2012 | Terumo Cardiovascular Systems Corp |
-