Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K230949 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| ARTIS Pheno VE30A and VE40A, Model 10849000 | 2 | 04/16/2026 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
| ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imag... | 2 | 06/27/2025 |
FEI # 2240869 Siemens Medical Solutions USA, Inc |
-







