FDA 510(k) Applications Submitted by Shlomi Deler

FDA 510(k) Number Submission Date Device Name Applicant
K191023 04/17/2019 Dolphin/IQ, Dolphin/4D and Dolphin/MAX Viasonix Ltd.
K221904 06/30/2022 EK12 V2 Algorithm GE Medical Systems Information Technologies, Inc.
K192607 09/20/2019 LiteWalk Viasonix Ltd.
K112754 09/21/2011 IVENT101 VERSAMED MEDICAL SYSTEMS LTD.
K123144 10/05/2012 VIVO 50 GE HEALTHCARE, BREAS MEDICAL AB


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