K240426
- 510(k) number
- K240426
- Device name
- Aventus Clot Management System
- Applicant
- Inquis Medical CA · US
- Product code
- CAC — Apparatus, Autotransfusion
- Decision date
- 2024-05-14
- Date received
- 2024-02-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K240426.pdf
Official FDA record: K240426
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.