Medical Device Recalls
-
1 result found
510(K) Number: K050794 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Possis AngioJet XVG Thrombectomy Sets, Model/Order # 105042-001, Sterilized with Ethylene Oxide, P... | 2 | 08/10/2007 | Possis Medical, Inc |
-