Medical Device Manufacturer · US , Dover , DE

Anx Robotica, Inc. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2020

1

Total

0

Cleared

1

Denied

Anx Robotica, Inc. has 0 FDA 510(k) cleared medical devices. Based in Dover, US.

Active since 2020. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Anx Robotica, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Anx Robotica, Inc.

1 devices

1-1 of 1

Not Cleared May 22, 2020

NaviCam Capsule Endoscope System with NaviCam Stomach Capsule

DEN190037 · QKZ

Gastroenterology & Urology · 283d