AI devices with FDA product code QEK — Angiographic Coronary Vascular Physiologic Simulation Software
Product code QEK (“Angiographic Coronary Vascular Physiologic Simulation Software” in openFDA) covers 2 devices on the FDA AI-enabled list, from 1 company. Most are reviewed by the Cardiovascular panel (2). The most recent decision was FFRangio on December 9, 2019.
2AI devices
1Companies
2018First decision
2019-12-09Latest decision
Trend: devices per year
20182019