K252284
- 510(k) number
- K252284
- Device name
- eMurmur Heart AI
- Applicant
- Csd Labs AT
- Product code
- DQD — Stethoscope, Electronic
- Decision date
- 2025-12-19
- Date received
- 2025-07-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 3.2 MB · U.S. public domain
Also available from FDA: K252284.pdf
Official FDA record: K252284
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.