FDA 510(k)

VoqX Electronic Stethoscope

Número K: K212709 · 2022-03-15

Data da decisão2022-03-15

Código do produtoDQD

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

VoqX Electronic Stethoscope is the device name listed in this FDA 510(k) record. The listed applicant is Sanolla , Ltd.. It received FDA 510(k) clearance on 2022-03-15 under 510(k) number K212709. 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 VoqX Electronic Stethoscope?

VoqX Electronic Stethoscope is a medical device that received FDA 510(k) clearance on 2022-03-15. The listed applicant is Sanolla , Ltd.. The 510(k) number is K212709.

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

VoqX Electronic Stethoscope received FDA 510(k) clearance on 2022-03-15, under 510(k) number K212709.

Who is the listed applicant for VoqX Electronic Stethoscope?

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

What is the FDA product code for VoqX Electronic Stethoscope?

The FDA product code for VoqX Electronic Stethoscope is DQD.

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