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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