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FDA 510(k) Applications Submitted by AnX Robotica Corporation
FDA 510(k) Number
Submission Date
Device Name
Applicant
K231960
07/03/2023
NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Capsule and NaviCam Tether
AnX Robotica Corporation
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