Medical Device Recalls
-
|
1 result found
510(K) Number: K111900 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| The Arrow Edge Hemodialysis Catheterization Set Long-Term Access and NextStep Antegrade Hemodialysis... | 2 | 01/22/2015 | Arrow International Inc |
-







