Medical Device Recalls
-
1 result found
510(K) Number: K122581 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
FlowGate Balloon Guide Catheter; Manufactured by Concentric Medical, Mountain View, CA. FlowGate... | 2 | 01/08/2013 | Concentric Medical Inc |
-