FDA 510(k) Applications Submitted by Viramed Biotech AG

FDA 510(k) Number Submission Date Device Name Applicant
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
K220016 01/05/2022 Viramed Borrela All-In-One ViraChip Test Kit Viramed Biotech AG
K163695 12/28/2016 Borrelia B31 ViraChip IgM Test Kit Viramed Biotech AG
K163504 12/14/2016 Borrelia B31 ViraChip IgG Test Kit VIRAMED BIOTECH AG


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