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FDA 510(k)

VasQ

N.º K: K240119 · 2024-02-16

SolicitanteLaminate Medical Technologies , Ltd.
Fecha de decisión2024-02-16
Código de productoQVQ
Comité asesorCV
DecisiónSubstantially Equivalent

Resumen del dispositivo

VasQ is the device name listed in this FDA 510(k) record. The listed applicant is Laminate Medical Technologies , Ltd.. It received FDA 510(k) clearance on 2024-02-16 under 510(k) number K240119. The device is classified under product code QVQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the VasQ?

VasQ is a medical device that received FDA 510(k) clearance on 2024-02-16. The listed applicant is Laminate Medical Technologies , Ltd.. The 510(k) number is K240119.

When did VasQ receive FDA 510(k) clearance?

VasQ received FDA 510(k) clearance on 2024-02-16, under 510(k) number K240119.

Who is the listed applicant for VasQ?

The FDA 510(k) record lists Laminate Medical Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VasQ?

The FDA product code for VasQ is QVQ.

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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