Medical Device Recalls
-
|
1 result found
510(K) Number: K934624 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| ACS Rotating Hemostatic Valve, .115 inch, for use with a dilatation catheter - Reference Number 2324... | 2 | 02/01/2007 | Abbott Vascular-Cardiac Therapies dba Guidant Corporation |
-







