Medical Device Recalls
-
1 result found
510(K) Number: K010737 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Medtronic Select CAP Arterial Cannulae. Vented, models 78818 (18 Fr.), 78820 (20 Fr.), 78822 (22 F... | 2 | 02/20/2014 | Medtronic Inc. Cardiac Rhythm Disease Management |
-