Medical Device Recalls
-
|
1 result found
PMA Number: P010031/S031 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Medtronic Concerto, C154DWK, Dual chamber implantable cardioverter defibrillator with cardiac resync... | 2 | 11/09/2009 |
FEI # 2182208 Medtronic Inc. Cardiac Rhythm Disease Managment |
-







