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FDA 510(k) Applications Submitted by Ventripoint Diagnostics, Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K191493
06/05/2019
Ventripoint Medical System Plus (VMS+) 3.0
Ventripoint Diagnostics, Ltd.
K173810
12/15/2017
Ventripoint Medical System Plus (VMS+)
Ventripoint Diagnostics, Ltd.
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