Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K974302 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| LIGHT DIAGNOSTICS Simulfluor Flu A / Flu B 2 mL Reagent Catalog # 5250 which is a component in the K... | 2 | 03/06/2009 |
FEI # 2024094 Millipore Corporation |
| LIGHT DIAGNOSTICS SimulFluor Flu A/Flu B DFA Kit Immunofluorescence Assay Cat. No. 3121 F... | 2 | 03/06/2009 |
FEI # 2024094 Millipore Corporation |
-







