FDA 510(k)

SonoStik Guide Wire Introducer

Número K: K243061 · 2024-11-04

Data da decisão2024-11-04

Código do produtoDYB

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

SonoStik Guide Wire Introducer is the device name listed in this FDA 510(k) record. The listed applicant is Sonostik, LLC. It received FDA 510(k) clearance on 2024-11-04 under 510(k) number K243061. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the SonoStik Guide Wire Introducer?

SonoStik Guide Wire Introducer is a medical device that received FDA 510(k) clearance on 2024-11-04. The listed applicant is Sonostik, LLC. The 510(k) number is K243061.

When did SonoStik Guide Wire Introducer receive FDA 510(k) clearance?

SonoStik Guide Wire Introducer received FDA 510(k) clearance on 2024-11-04, under 510(k) number K243061.

Who is the listed applicant for SonoStik Guide Wire Introducer?

The FDA 510(k) record lists Sonostik, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SonoStik Guide Wire Introducer?

The FDA product code for SonoStik Guide Wire Introducer is DYB.

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Dispositivos Relacionados (Código: DYB)

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Fonte oficial

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