Medical Device Recalls
-
1 result found
510(K) Number: K063643 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Bio-Rad Variant II Hemoglobin Testing System with CDM v 4.0, model number 270-2000, Manufactured by ... | 2 | 05/19/2009 | Bio-Rad Laboratories Inc |
-