QZW — Over-The-Counter Device To Assess Risk Of Sleep Apnea Class II

FDA Device Classification

Classification Details

Product Code
QZW
Device Class
Class II
Regulation Number
868.2378
Submission Type
Review Panel
AN
Medical Specialty
Anesthesiology
Implant
No

Definition

An over-the-counter device to assess risk of sleep apnea is intended to provide a notification of the risk of sleep apnea in users who have not been previously diagnosed with sleep apnea. This device uses software algorithms to analyze input sensor signals and provide a risk assessment for sleep apnea. It is not intended to provide a standalone diagnosis, replace traditional methods of diagnosis (e.g., polysomnography), assist clinicians in diagnosing sleep disorders, or be used as an apnea monitor.

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K240929appleSleep Apnea Notification Feature (SANF)September 13, 2024
DEN230041samsung electronics coSleep Apnea FeatureFebruary 6, 2024