Medical Device Recalls
-
1 result found
510(K) Number: K202141 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Scorpion Portal Vein Access Set - Product Usage: used to gain access to the hepatic vein and guide a... | 2 | 09/21/2021 | Argon Medical Devices, Inc |
-