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FDA 510(k)

Aventus Clot Management System

K-Number: K240426 · 2024-05-14

Decision Date2024-05-14
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Aventus Clot Management System is a medical device manufactured by Inquis Medical. It received FDA 510(k) clearance on 2024-05-14 under approval number K240426. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Aventus Clot Management System?

Aventus Clot Management System is a medical device that received FDA 510(k) clearance on 2024-05-14. It is manufactured by Inquis Medical. The 510(k) number is K240426.

When was Aventus Clot Management System approved by the FDA?

Aventus Clot Management System received FDA 510(k) clearance on 2024-05-14, under approval number K240426.

What company makes Aventus Clot Management System?

Aventus Clot Management System is manufactured by Inquis Medical.

What is the FDA product code for Aventus Clot Management System?

The FDA product code for Aventus Clot Management System is CAC.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.