QZWClass II
Over-the-counter Device To Assess Risk Of Sleep Apnea
Anesthesiology · 21 CFR 868.2378
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.
MDR events2All time
Recalls0All time
Registered firms2Currently listed
510(k) clearances3All time
Recent MDR events
2 adverse event reports on file
Event type breakdown
Injury1
Malfunction1
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
2 firms currently registered for this product code