meddevicedb.com FDA Device Reference

Hypertension Prediction Index (HePI) Algorithm

K242518 Class II Traditional
Decision Date
2025-05-15
Sponsor / Applicant
Edwards Lifesciences, LLC

Technical Specification

510(k) Submission ID K242518
Product Code QAQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2210
Decision Date 2025-05-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Hypertension Prediction Index (HePI) Algorithm received FDA 510(k) clearance under submission number K242518, sponsored by Edwards Lifesciences, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2025-05-15.

Classification & Regulation

This clearance is catalogued under FDA product code QAQ and 21 CFR 870.2210, within the Cardiovascular review panel as a Class II device.