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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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