K262030
- 510(k) number
- K262030
- Device name
- Aventus Thrombectomy System
- Applicant
- Inquis Medical CA · US
- Product code
- QEZ — Aspiration Thrombectomy Catheter
- Decision date
- 2026-07-15
- Date received
- 2026-06-17
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K262030.pdf
Official FDA record: K262030
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.