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FDA 510(k) Applications Submitted by CHRISTOPHER BENSTEN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K041658
06/18/2004
BIOPLEX 200 ANA SCREEN ON THE BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM, MODEL BIOPLEX 2200
BIO-RAD LABORATORIES, INC.
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