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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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