K233872
- 510(k) number
- K233872
- Device name
- Daylight
- Applicant
- Big Health, Inc. CA · US
- Product code
- SCP — Computerized Behavioral Therapy Device For Anxiety D
- Decision date
- 2024-08-30
- Date received
- 2023-12-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K233872.pdf
Official FDA record: K233872
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.