FDA 510(k) Applications Submitted by Martin Kintrup

FDA 510(k) Number Submission Date Device Name Applicant
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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