Medical Device Recalls
-
1 result found
510(K) Number: K060973 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Vycor Medical ViewSite Brain Access System 17mm/ 11mm / 5cm Device***STERILE*** Product Usage: T... | 1 | 01/17/2013 | Vycor Medical, Inc. |
-