AI devices with FDA product code SDY — Loss Of Pulse Notification Software
Product code SDY (“Loss Of Pulse Notification Software” in openFDA) covers 1 device on the FDA AI-enabled list, from 1 company. Most are reviewed by the Cardiovascular panel (1). The most recent decision was Loss of Pulse Detection on February 25, 2025.
1AI devices
1Companies
2025First decision
2025-02-25Latest decision
Trend: devices per year
2025