FDA 510(k) Applications Submitted by Jennifer Jines

FDA 510(k) Number Submission Date Device Name Applicant
K181412 05/30/2018 VITEK MS bioMerieux, Inc.
K192110 08/05/2019 Vitek Densichek bioMerieux, Inc
K163006 10/28/2016 VITEK 2 AST-GN Tigecycline (<0.5->8 ug/mL) bioMerieux, Inc.


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