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FDA 510(k) Applications Submitted by Hans Bostrom
FDA 510(k) Number
Submission Date
Device Name
Applicant
K122149
07/19/2012
QBTES
QBTECH AB
K133382
11/04/2013
QB TEST
QBTECH AB
K143468
12/04/2014
QbCheck
QBTECH AB
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