Medical Device Recalls
-
1 result found
510(K) Number: K970886 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Maquet Blueline Series 30/80 OR Light Systems, Model Numbers and Catalog Numbers BLUE 30 - ARD569015... | 2 | 01/19/2024 | Getinge Usa Sales Inc |
-