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FDA 510(k) Applications Submitted by Motus GI Medical Technologies Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K160015
01/04/2016
Pure Vu
Motus GI Medical Technologies Ltd.
K181437
06/01/2018
Pure Vu System
Motus GI Medical Technologies Ltd.
K173392
10/30/2017
Pure-Vu System
Motus GI Medical Technologies Ltd.
K220007
01/04/2022
Pure-Vu EVS System
Motus GI Medical Technologies Ltd.
K210981
04/01/2021
Pure Vu System
Motus GI Medical Technologies Ltd.
K191220
05/07/2019
Pure Vu System
Motus GI Medical Technologies Ltd.
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