K240119
- 510(k) number
- K240119
- Device name
- VasQ
- Applicant
- Laminate Medical Technologies , Ltd. IL
- Product code
- QVQ — Extravascular Support For An Arteriovenous Fistula F
- Decision date
- 2024-02-16
- Date received
- 2024-01-16
- 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: K240119.pdf
Official FDA record: K240119
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.