Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K913120 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
POLYSTAR T.O.P., Angiographic X-Ray System, Model Numbers 1148902 and 4784505. | 3 | 11/16/2004 | Siemens Medical Solutions USA, Inc |
POLYSTAR, Angiographic X-Ray System, Model 1148902 | 3 | 11/16/2004 | Siemens Medical Solutions USA, Inc |
-