Medical Device Recalls
-
|
1 result found
510(K) Number: K811268 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Transfer Device, REF 2008S. Packaged on a form, fill and seal machine with a poly/Tyvek material the... | 2 | 08/16/2024 |
FEI # 3014342658 Microtek Medical Inc. |
-







