Known Identifiers & Locations
FEI Numbers
3002698356
Owner Operator Numbers
N/A
Locations Covered
N/A
Registered Establishments (0)
No device registration and listing records found for this entity.
510(k) Premarket Notifications (0)
No 510(k) notifications found for this entity.
FDA Recall History (2)
| Recall # |
Product Description |
Initiation Date |
Status |
Action |
| Z-0002-05 |
Automated Differential Cell Counter
Reason: Device can generate overestimated platelet results.
|
2004-08-13 |
Terminated
|
View Details
|
| Z-0003-05 |
Automated Differential Cell Counter
Reason: Device can generate overestimated platelet results.
|
2004-08-13 |
Terminated
|
View Details
|
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