AI devices with FDA product code PIW — Brain Injury Adjunctive Interpretive Electroencephalograph Assessment Aid
Product code PIW (“Brain Injury Adjunctive Interpretive Electroencephalograph Assessment Aid” in openFDA) covers 4 devices on the FDA AI-enabled list, from 4 companies. Most are reviewed by the Neurology panel (4). The most recent decision was BrainScope TBI on September 11, 2019.
4AI devices
1Companies
2014First decision
2019-09-11Latest decision
Trend: devices per year
2014201520162019