FDA 510(k)

Liberant™ RX Aspiration Catheter

N.º K: K253589 · 2026-04-23

SolicitanteMedtronic Interventional Vascular, Inc.

Fecha de decisión2026-04-23

Código de productoQEZ

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

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.

Preguntas frecuentes

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.

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Fuente oficial

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