Anx Robotica Corporation
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories3
Latest Approval2025-05-21
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K250493 | MotiliCap GI Monitoring System | NYV | 2025-05-21 | View |
| 510(k) | K233229 | NaviCam Small Bowel Capsule Endoscopy System with NaviCam SB Capsule and NaviCam Tether | NEZ | 2024-01-05 | View |
| 510(k) | K231960 | NaviCam Xpress Stomach Capsule Endoscope System (NaviCam Xpress Stomach System) with NaviCam Capsule and NaviCam Tether | QKZ | 2023-10-03 | View |
No matching devices.