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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