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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