Medical Device Recalls
-
1 result found
510(K) Number: K093455 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
CARTO 3 Systems, Product Code M-4800-01 The intended use of the CARTO 3 System is catheter-based ... | 2 | 03/20/2012 | Biosense Webster, Inc. |
-