FDA 510(k)

LinkQuest Diagnostic Ultrasound System model SQ860

Número K: K172059 · 2017-10-05

Data da decisão2017-10-05

Código do produtoIYN

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

LinkQuest Diagnostic Ultrasound System model SQ860 is the device name listed in this FDA 510(k) record. The listed applicant is Linkquest, Inc.. It received FDA 510(k) clearance on 2017-10-05 under 510(k) number K172059. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the LinkQuest Diagnostic Ultrasound System model SQ860?

LinkQuest Diagnostic Ultrasound System model SQ860 is a medical device that received FDA 510(k) clearance on 2017-10-05. The listed applicant is Linkquest, Inc.. The 510(k) number is K172059.

When did LinkQuest Diagnostic Ultrasound System model SQ860 receive FDA 510(k) clearance?

LinkQuest Diagnostic Ultrasound System model SQ860 received FDA 510(k) clearance on 2017-10-05, under 510(k) number K172059.

Who is the listed applicant for LinkQuest Diagnostic Ultrasound System model SQ860?

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

What is the FDA product code for LinkQuest Diagnostic Ultrasound System model SQ860?

The FDA product code for LinkQuest Diagnostic Ultrasound System model SQ860 is IYN.

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Dispositivos Relacionados (Código: IYN)

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