K252595
- 510(k) number
- K252595
- Device name
- Stethophone Pro
- Applicant
- Sparrow Acoustics, Inc. CA
- Product code
- DQD — Stethoscope, Electronic
- Decision date
- 2025-09-12
- Date received
- 2025-08-15
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K252595.pdf
Official FDA record: K252595
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.