Medical Device Recalls
-
1 result found
510(K) Number: K163334 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
CM 50-001-01 Injectate Kit, accessory device to LiDCOunity v2 Monitor - Product Usage: intended to a... | 2 | 12/30/2020 | Lidco Ltd |
-