Medical Device Recalls
-
|
1 result found
510(K) Number: K953868 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other n... | 2 | 08/22/2018 |
FEI # 3002808001 Richard Wolf GmbH |
-







