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FDA 510(k) Applications Submitted by Bonnie B 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
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