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Anx Robotica Corporation

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K250493 MotiliCap GI Monitoring SystemNYV2025-05-21 View
510(k) K233229 NaviCam Small Bowel Capsule Endoscopy System with NaviCam SB Capsule and NaviCam TetherNEZ2024-01-05 View
510(k) K231960 NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Capsule and NaviCam TetherQKZ2023-10-03 View
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