K223515
- 510(k) number
- K223515
- Device name
- MamaLift Plus
- Applicant
- Curio Digital Therapeutics, Inc. NJ · US
- Product code
- SAP — Computerized Behavioral Therapy Device For Depressiv
- Decision date
- 2024-04-22
- Date received
- 2022-11-22
- 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: K223515.pdf
Official FDA record: K223515
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.