Medical Device Recalls
-
1 result found
510(K) Number: K001577 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Outback LTD Re-Entry Catheter, Sterile, Single Use. The Cordis LuMend OUTBACK LTD Re-Entry Catheter... | 2 | 10/31/2008 | Cordis Corporation |
-