Medical Device Recalls
-
|
1 result found
510(K) Number: K030415 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| MORPHEUS CT PICC with STYLET, 5F Dual Lumen 65 cm Insertion Kit, Catalog No./REF 1200923, STERILE, ... | 3 | 01/11/2012 |
FEI # 3008319439 Angiodynamics Worldwide Headquarters |
-







