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FDA 510(k) Applications Submitted by DAVID BHEND
FDA 510(k) Number
Submission Date
Device Name
Applicant
K091616
06/03/2009
BIOPLEX 2200 MMRV IGG
Bio-Rad Laboratories
K062211
08/01/2006
BIOPLEX 2200 EBV IGG PANEL FOR BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM
BIO-RAD LABORATORIES, INC.
K062213
08/01/2006
BIOPLEX 2200 EBV IGM PANEL ON BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM
BIO-RAD LABORATORIES, INC.
K063866
12/29/2006
BIOPLEX 2200 SYPHILIS IGG KIT ON THE BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM
Bio-Rad Laboratories
K090409
02/18/2009
BIOPLEX 2200 HSV-1 AND HSV-2 IGG ON THE BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM
Bio-Rad Laboratories
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