Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K830233 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Leonard 10.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth Cuff with Peel-Apart Percutane... | 2 | 03/06/2013 | Bard Access Systems |
Hickman 9.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth Cuff with Peel-Apart Percutaneo... | 2 | 03/06/2013 | Bard Access Systems |
-