Last synced on 18 April 2025 at 11:05 pm

Gastrointestinal Capsule Endoscopy Analysis Software Device

Page Type
Product Code
Definition
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.
Physical State
The subject device is not physical. It is software.
Technical Method
The subject device uses convolution neural networks to provide AI-enabled clinician feedback for identifying potential lesions and determine the anatomical tract site being visualized.
Target Area
Gastrointestinal tract
Regulation Medical Specialty
Gastroenterology and Urology
Review Panel
Gastroenterology and Urology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
876.1540
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QZF is linked to regulation 21CFR876.1540, which does not seem to exist yet. It may be pending at the moment.

Gastrointestinal Capsule Endoscopy Analysis Software Device

Page Type
Product Code
Definition
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.
Physical State
The subject device is not physical. It is software.
Technical Method
The subject device uses convolution neural networks to provide AI-enabled clinician feedback for identifying potential lesions and determine the anatomical tract site being visualized.
Target Area
Gastrointestinal tract
Regulation Medical Specialty
Gastroenterology and Urology
Review Panel
Gastroenterology and Urology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
876.1540
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QZF is linked to regulation 21CFR876.1540, which does not seem to exist yet. It may be pending at the moment.