Medical Device Recalls
-
|
1 to 2 of 2 Results
510(K) Number: K120771 |
|
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| UniCel DxH 600 COULTER Cellular Analysis System, configured with the Led HGB Photometer REF:B23858 | 2 | 09/17/2025 |
FEI # 2050012 Beckman Coulter Inc. |
| UniCel DxH 800 and DxH 600 Coulter Cellular Analysis Systems The UniCel DxH 800/DxH 600 analyzers... | 2 | 11/04/2013 |
FEI # 2050012 Beckman Coulter Inc. |
-







