K250202
- 510(k) number
- K250202
- Device name
- Aventus Thrombectomy System
- Applicant
- Inquis Medical CA · US
- Product code
- QEW — Peripheral Mechanical Thrombectomy With Aspiration
- Decision date
- 2025-02-26
- Date received
- 2025-01-24
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.5 MB · U.S. public domain
Also available from FDA: K250202.pdf
Official FDA record: K250202
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.