Medical Device Recalls
-
1 result found
510(K) Number: K123553 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified profes... | 2 | 02/14/2018 | Zimmer Surgical Inc |
-