Business · 13/12/2021Updated: 10/17/2026 · 1 min read
FDA Classifies Pressure Ulcer Management Tool as Class I Device
Summary
The US Food and Drug Administration has classified the pressure ulcer management tool as a Class I device, which will provide a reasonable assurance of its safety and effectiveness, and enhance patients' access to innovative devices.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →