Medical Device Recalls
-
1 result found
510(K) Number: K132829 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Quadrox-iD Adult Diffusion Membrane Oxygenator Product Usage: The Quadrox-iD Adult Diffusion Mem... | 2 | 05/28/2015 | Maquet Cardiovascular Us Sales, Llc |
-