Medical Device Recalls
-
1 result found
510(K) Number: K961405 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Pulstar(R) DVT PREVENTION SYSTEM, Anti-Embolism Wrap System, albahealth(R), A Subsidiary of Encompas... | 2 | 11/14/2011 | Albahealth LLC |
-