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FDA 510(k) Applications Submitted by BARRY MENEFEE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K960182
01/16/1996
DSDNA IMMUNOGLOBULIN EIA TEST SYSTEM
MARDX DIAGNOSTICS, INC.
K092693
09/02/2009
VIRAMED BIOTECH AG BORRELIA B31 IGG VIRASTRIPE, MODEL V-BBSGUS
VIRAMED BIOTECH AG
K051071
04/26/2005
VIRAMED BIOTECH BORRELIA B31 IGG VIRABLOT
VIRAMED BIOTECH AG
K051169
04/29/2005
BIRAMED BIOTECH BORRELIA B31 IGM VIRABLOT
VIRAMED BIOTECH AG
K082329
08/14/2008
VIRAMED BIOTECH AG BORRELIA B31 IGM VIRASTRIPE
VIRAMED BIOTECH AG
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