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FDA 510(k) Applications Submitted by Patricia Dupe
FDA 510(k) Number
Submission Date
Device Name
Applicant
K141728
06/26/2014
ACE CALIBRATOR
SENTINEL CH. SpA
K192118
08/06/2019
CRP Vario
Sentinel CH, Spa
K193001
10/28/2019
Albumin BCP
Sentinel CH. SpA
K173833
12/18/2017
CRP Vario
SENTINEL CH. SpA
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