Medical Device Recalls
-
1 result found
510(K) Number: K034050 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***REF Cat. No.***466F220A and 466F220B***Ve... | 1 | 08/07/2013 | Cordis Corporation |
-