FDA 510(k)

LigaPASS™ System

N.º K: K261374 · 2026-05-27

Fecha de decisión2026-05-27

Código de productoOWI

Comité asesorOR

DecisiónSubstantially Equivalent

Resumen del dispositivo

LigaPASS™ System is the device name listed in this FDA 510(k) record. The listed applicant is Medicrea International S.A.S. It received FDA 510(k) clearance on 2026-05-27 under 510(k) number K261374. The device is classified under product code OWI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the LigaPASS™ System?

LigaPASS™ System is a medical device that received FDA 510(k) clearance on 2026-05-27. The listed applicant is Medicrea International S.A.S. The 510(k) number is K261374.

When did LigaPASS™ System receive FDA 510(k) clearance?

LigaPASS™ System received FDA 510(k) clearance on 2026-05-27, under 510(k) number K261374.

Who is the listed applicant for LigaPASS™ System?

The FDA 510(k) record lists Medicrea International S.A.S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LigaPASS™ System?

The FDA product code for LigaPASS™ System is OWI.

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Fuente oficial

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