Medical Device Recalls
-
|
1 result found
510(K) Number: K113679 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Maquet Lucea - Lucea10/40, Lucea50/100 OR Light Systems, Model Numbers and Catalog Numbers LCA 10 - ... | 2 | 01/19/2024 |
FEI # 3013876692 Getinge Usa Sales Inc |
-







