Medical Device Recalls
-
1 result found
510(K) Number: K041453 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
LeMaitre Vascular Tumescent Catheter Inversion (TCI) System. The TCI System is intended to provid... | 3 | 03/18/2015 | LeMaitre Vascular, Inc. |
-