OQU

Airway Monitoring System

Product code

OQU

Device name

Airway Monitoring System

Device class

Class 2

21 CFR

21 CFR 868.5730

Medical specialty

Anesthesiology

Marketing pathway

510(K)

510(k) clearances (all years, FDA)

3 (all years; only the last 3 years are listed here)

FDA classification definition

The device is intended to assist in verifying ett tube placement, assist in detecting ett tube movement and obstruction of the tube tip

Definition text from the FDA device classification database (U.S. federal government work, public domain).