Medical Device Recalls
-
|
1 result found
510(K) Number: K896294 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| Active INTACT PTH, Part Number: DSL-8000 The DSL-80000 ACTIVE Intact PTH IRMA Kit provides material... | 2 | 12/09/2010 | Beckman Coulter Inc. |
-







