Medical Device Recalls
-
1 result found
510(K) Number: K982879 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Data reduction program written for a specific automated microtiter plate instrument (Bio-Tek ELx800)... | 3 | 04/06/2005 | Diasorin Inc. |
-