Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K022161 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Coulter LH 750, Coulter LH 780, and Coulter LH 500 Analyzers Hematology Analyzers are quantitative,... | 2 | 09/07/2017 | Beckman Coulter Inc. |
COULTER LH 700 Series Hematology Analyzers | 2 | 01/09/2003 | Beckman Coulter Inc |
-