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Devices · Analytics for Life, Inc.

CorVista System with PH Add-On

510(k)K233666CardiovascularSAT

Analytics for Life, Inc. is listed for CorVista System with PH Add-On (K233666). The FDA list gives April 5, 2024 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 SAT as “Pulmonary Hypertension Machine Learning-Based Notification Software”: Pulmonary hypertension machine learning-based notification software employs machine learning techniques to suggest the likelihood of pulmonary hypertension 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=K233666

Official FDA database record

Date of final decision
April 5, 2024
Company on the FDA list
Analytics for Life, Inc.
Lead panel
Cardiovascular
Primary product code
SAT
openFDA device name for the code
Pulmonary Hypertension 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

Product-code text from openFDA

Pulmonary hypertension machine learning-based notification software employs machine learning techniques to suggest the likelihood of pulmonary hypertension for further referral or diagnostic follow-up.