Medical Device Recalls
-
1 result found
510(K) Number: K123314 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
The Affinity Fusion Oxygenator with Integrated Arterial Filter and Carmeda Bioactive Surface is a si... | 2 | 12/16/2014 | Medtronic Perfusion Systems |
-