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FDA 510(k) Applications Submitted by Visionsense Ltd.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K150018
01/05/2015
VS3-IR-MMS System
Visionsense Ltd.
K171208
04/25/2017
Trans-anal Introducer
Visionsense Ltd.
K223020
09/29/2022
VS3-Iridium System (VS3-IR)
Visionsense Ltd.
K210265
02/01/2021
VS3 Iridium Sytem
Visionsense Ltd.
K141002
04/18/2014
VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
Visionsense Ltd.
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