FDA 510(k) Applications Submitted by BONNIE DEJOY

FDA 510(k) Number	Submission Date	Device Name	Applicant
K033051	09/29/2003	LEGIONELLA PNEUMOPHILA IGG/IGM	TRINITY BIOTECH USA
K033059	09/29/2003	HERPES GROUP IGG	TRINITY BIOTECH, INC.
K033105	09/30/2003	CAPTIA HSV 1 IGG TYPE SPECIFIC ELISA KIT	TRINITY BIOTECH USA
K140455	02/24/2014	CAPTIA MEASLES IGM	TRINITY BIOTECH USA
K033064	09/29/2003	MYCOPLASMA IGG	TRINITY BIOTECH USA
K033067	09/29/2003	PYLORI IGG	TRINITY BIOTECH USA
K033070	09/29/2003	BORRELIA BURGDORFERI IGM ELISA TEST SYSTEM	TRINITY BIOTECH USA
K033079	09/29/2003	CHLAMYDIA IGG ELISA TEST SYSTEM	TRINITY BIOTECH USA
K033083	09/29/2003	BORRELIA BURGDORFERI IGG/IGM ELISA TEST SYSTEM	TRINITY BIOTECH USA
K033106	09/30/2003	CAPTIA HSV 2 IGG TYPE SPECIFIC ELISA KIT	TRINITY BIOTECH USA
K083896	12/29/2008	DESTINY MAX COAGULATION ANALYZER	TRINITY BIOTECH