510(k) K240426

Device
Aventus Clot Management System
Applicant
Inquis Medical
510(k) number
K240426
Product code
CAC
Decision
Substantially Equivalent (SESE)
Decision date
2024-05-14
Date received
2024-02-13
Regulation
868.5830
Classification name
Apparatus, Autotransfusion
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Mojgan Sadaat
Address
127 Independence Dr. Menlo Park CA US 94025 94025

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Related GUDID Devices

Primary DIBrandCompanyPublished
00860009303416Aventus Thrombectomy System - Clot Management SystemInquis Medical, Inc.2024-07-23

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