K240901
- 510(k) number
- K240901
- Device name
- Stethophone
- Applicant
- Sparrow Acoustics, Inc. CA
- Product code
- DQD — Stethoscope, Electronic
- Decision date
- 2024-09-19
- Date received
- 2024-04-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 3.3 MB · U.S. public domain
Also available from FDA: K240901.pdf
Official FDA record: K240901
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.