Medical Device Recalls
-
|
141 to 141 of 141 Results
510(K) Number: K022947 |
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| 100/120V AC, Advanced Perfusion System Platform (APS) The Terumo® Advanced Perfusion System 1 is ind... | 2 | 05/28/2015 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
-







