Medical Device Recalls
-
21 to 21 of 21 Results
510(K) Number: K021021 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Axiom Artis dBA, Axiom Artis Modular Angiography X-Ray System, Model number 7555357. | 2 | 11/25/2008 | Siemens Medical Solutions USA, Inc |
-