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FDA 510(k) Applications Submitted by AnX Robotica Corp
FDA 510(k) Number
Submission Date
Device Name
Applicant
K203192
10/28/2020
NaviCam Xpress Stomach System
AnX Robotica Corp
K221608
06/03/2022
NaviCam Capsule Endoscope System with NaviCam Stomach Capsule and NaviCam Tether, NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach Capsule and NaviCam Tether
AnX Robotica Corp
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