Devices · CorVista Health, Inc.

CorVista® System

CorVista Health, Inc. is listed for CorVista® System (K232686). The FDA list gives September 8, 2023 as the date of the final decision. The lead panel is Cardiovascular, and the database link on the FDA list is the 510(k) pathway. openFDA describes product code QXX as “Coronary Artery Disease Machine Learning-Based Notification Software”: Coronary Artery Disease machine learning-based notification software employs machine learning techniques to suggest the likelihood of coronary artery disease for further referral or diagnostic follow-up. openFDA records this submission’s decision description as “Substantially Equivalent.” This paragraph is assembled only from those public fields. It is not an FDA review, not a determination of safety or effectiveness, and not medical advice. Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K232686

Official FDA database record

Date of final decision

September 8, 2023

Company on the FDA list

CorVista Health, Inc.

Lead panel

Cardiovascular

Primary product code

QXX

openFDA device name for the code

Coronary Artery Disease Machine Learning-Based Notification Software

Device class

2

Regulation number

870.2380

openFDA decision description

Substantially Equivalent

openFDA decision code

SESE

Statement or summary label

Summary