Medical Device Recalls
-
|
1 result found
510(K) Number: K934937 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Axillent Debakey Grasping Forceps, Part No. 33821DYD In general the surgeons use 33821DYD Debakey... | 2 | 12/06/2013 |
FEI # 2020550 Karl Storz Endoscopy America Inc |
-







