K252076
- 510(k) number
- K252076
- Device name
- Kneevoice Cartilage Evaluation System (750-3600-001)
- Applicant
- Kneevoice, Inc. CA · US
- Product code
- DQD — Stethoscope, Electronic
- Decision date
- 2026-02-06
- Date received
- 2025-07-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K252076.pdf
Official FDA record: K252076
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.