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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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