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FDA 510(k)

Liberant™ RX Aspiration Catheter

K-Number: K253589 · 2026-04-23

ApplicantMedtronic Interventional Vascular, Inc.
Decision Date2026-04-23
Product CodeQEZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Liberant™ RX Aspiration Catheter is a medical device manufactured by Medtronic Interventional Vascular, Inc.. It received FDA 510(k) clearance on 2026-04-23 under approval number K253589. The device is classified under product code QEZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Liberant™ RX Aspiration Catheter?

Liberant™ RX Aspiration Catheter is a medical device that received FDA 510(k) clearance on 2026-04-23. It is manufactured by Medtronic Interventional Vascular, Inc.. The 510(k) number is K253589.

When was Liberant™ RX Aspiration Catheter approved by the FDA?

Liberant™ RX Aspiration Catheter received FDA 510(k) clearance on 2026-04-23, under approval number K253589.

What company makes Liberant™ RX Aspiration Catheter?

Liberant™ RX Aspiration Catheter is manufactured by Medtronic Interventional Vascular, Inc..

What is the FDA product code for Liberant™ RX Aspiration Catheter?

The FDA product code for Liberant™ RX Aspiration Catheter is QEZ.

Related Clinical Trials

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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.

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