FDA Device Recall
Cytomics FC 500 Flow Cytometry System with CXP Software Version 2.1 and 2.2 - SW Kit, CXP Analyis SW V2.2 Single User U…
- Recall Number
- Z-2027-2008
- CFRES ID
- 67143
- Firm
- Beckman Coulter Inc
- Status
- Terminated
- Initiated
- May 4, 2007
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Source: https://healthaicentral.com/research/regulatory-clearance/recalls/67143