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