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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 the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Interventional Vascular, Inc.. It received FDA 510(k) clearance on 2026-04-23 under 510(k) 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. The listed applicant is Medtronic Interventional Vascular, Inc.. The 510(k) number is K253589.

When did Liberant™ RX Aspiration Catheter receive FDA 510(k) clearance?

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

Who is the listed applicant for Liberant™ RX Aspiration Catheter?

The FDA 510(k) record lists Medtronic Interventional Vascular, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Devices (Code: QEZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261105Powered Aventus Thrombectomy System™Inquis MedicalK262030Aventus Thrombectomy SystemInquis MedicalK254208FLOWRUNNER Aspiration SystemExpanse Medical, Inc.K253925Aventus Thrombectomy SystemInquis MedicalK252509AlphaVac Multipurpose Mechanical Aspiration System F1885AngioDynamics, Inc.K251312Vesalio Peripheral SystemVesalio, Inc.

Official Source

View on FDA Database →

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

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