Medical Device Recalls
-
1 result found
510(K) Number: K082677 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Elevate® System with IntePro® Lite", Anterior and Apical Prolapse Repair System, REF720093-01, Steri... | 2 | 07/07/2011 | American Medical Systems, Inc. |
-