Medical Device Recalls
-
|
1 result found
510(K) Number: K150082 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A, View Station Software Kit 002... | 2 | 01/29/2016 |
FEI # 2221819 Mindray DS USA, Inc. dba Mindray North America |
-







