FDA 510(k)

Adscope 658 Estetoscópio Eletrônico

Número K: K162589 · 2017-03-10

Data da decisão2017-03-10

Código do produtoDQD

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

Adscope 658 Electronic Stethoscope is the device name listed in this FDA 510(k) record. The listed applicant is American Diagnostic Corp.. It received FDA 510(k) clearance on 2017-03-10 under 510(k) number K162589. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Adscope 658 Electronic Stethoscope?

Adscope 658 Electronic Stethoscope is a medical device that received FDA 510(k) clearance on 2017-03-10. The listed applicant is American Diagnostic Corp.. The 510(k) number is K162589.

When did Adscope 658 Electronic Stethoscope receive FDA 510(k) clearance?

Adscope 658 Electronic Stethoscope received FDA 510(k) clearance on 2017-03-10, under 510(k) number K162589.

Who is the listed applicant for Adscope 658 Electronic Stethoscope?

The FDA 510(k) record lists American Diagnostic Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Adscope 658 Electronic Stethoscope?

The FDA product code for Adscope 658 Electronic Stethoscope is DQD.

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