Medical Device Recalls
-
|
1 result found
510(K) Number: K933652 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Freedom60 Precision Flow Rate Tubing Sets, REF/Part Numbers F900, F2400, F60, F10, F275, F600, F45, ... | 2 | 01/05/2018 |
FEI # 1318360 Repro-Med Systems, Inc. |
-







