Medical Device Recalls
-
|
1 result found
510(K) Number: K071277 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Beckman Coulter Synchron AQUA CAL Level 1, Part No. 471288 Product Usage: Used for the system ca... | 2 | 07/13/2017 |
FEI # 2050012 Beckman Coulter Inc |
-







