AI devices with FDA product code MHX — Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Product code MHX (“Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)” in openFDA) covers 3 devices on the FDA AI-enabled list, from 2 companies. Most are reviewed by the Cardiovascular panel (3). The most recent decision was Corvair Monza on January 9, 2026.
3AI devices
2Companies
2008First decision
2026-01-09Latest decision
Trend: devices per year
200820242026