Medical Device Recalls
-
1 result found
510(K) Number: K010744 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Flowtron Trio DVT Pump; an Rx intermittent pneumatic compression deep vein thrombosis pump; ArjoHunt... | 2 | 12/27/2012 | Arjo, Inc. dba ArjoHuntleigh |
-