K240929
- 510(k) number
- K240929
- Device name
- Sleep Apnea Notification Feature (SANF)
- Applicant
- Apple, Inc. CA · US
- Product code
- QZW — Over-The-Counter Device To Assess Risk Of Sleep Apne
- Decision date
- 2024-09-13
- Date received
- 2024-04-04
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K240929.pdf
Official FDA record: K240929
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.