FDA 510(k) Applications Submitted by BECKMAN COULTER CELLULAR
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100489 | 02/19/2010 | DXH 300 COULTER CELLULAR ANALYSIS SYSTEM, DXH 300C COULTER CELLULAR ANALYSSI SYSTEM MODEL: 71772, 71771 | BECKMAN COULTER CELLULAR |
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