Medical Device Recalls
-
|
1 result found
510(K) Number: K925016 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Prep shave kit, catalog# 900-030 | 2 | 03/21/2012 | Customed, Inc |
-







