Medical Device Recalls
-
|
1 result found
510(K) Number: K072232 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Polyflux Revaclear, Capillary Dialyzer, Model Number 110633; Gambro Renal Products, Inc. Intende... | 2 | 05/21/2014 | Gambro Renal Products, Incorporated |
-







