Gastroenterology_urology

NaviCam ProScan

Ankon Technologies co., ltd

FDA-cleared AI medical device

A gastrointestinal capsule endoscopy analysis software device is used to analyze pre-recorded capsule endoscopy videos of the gastrointestinal tract that are suspected of containing lesions. This device uses software algorithms to identify images and areas of interest as outputs to aid the clinician in analyzing suspected lesions, for clinician review of device outputs. The device may contain hardware to support interfacing with a capsule imaging system.

FDA Submission Metadata

Submission number
DEN230027
Decision date
December 2023
FDA panel
Gastroenterology-Urology
Product code
QZF

This entry is sourced from the FDA AI/ML-Enabled Medical Devices list. No editorial review yet — the catalogue may add a deeper review of this device in future.

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