Medical Device Recalls
-
|
1 result found
510(K) Number: K032342 |
|
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. |
-







