Anx Robotica Corp
Anx Robotica Corp holds FDA 510(k) medical device clearances, first cleared 2019, most recent 2024.
Top product codes for Anx Robotica Corp
Recent clearances by Anx Robotica Corp
- K241934 — NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Stomach Capsule/Tether (NaviCam Xpress Stomach System with NaviCam Capsule/Tether)
- K230694 — NaviCam Xpress Stomach System, NaviCam Xpress System
- K221608 — 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
- K203192 — NaviCam Xpress Stomach System
- K201106 — IntraMarX 3D Radiopaque Marker
- K191087 — IntraMarX Radiopaque Markers
Data sourced from openFDA. This site is unofficial and independent of the FDA.