K233976
- 510(k) number
- K233976
- Device name
- VasoGuard (V10, V8, V6, V4, V2)
- Applicant
- Corvascular Diagnostics, LLC MN · US
- Product code
- JOP — Transducer, Ultrasonic
- Decision date
- 2024-07-19
- Date received
- 2023-12-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.6 MB · U.S. public domain
Also available from FDA: K233976.pdf
Official FDA record: K233976
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.