FDA 510(k)

ibiomedi Electronic Stethoscope ES-2020

Número K: K220466 · 2022-11-03

Data da decisão2022-11-03

Código do produtoDQD

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

ibiomedi Electronic Stethoscope ES-2020 is the device name listed in this FDA 510(k) record. The listed applicant is Sound Land Corp.. It received FDA 510(k) clearance on 2022-11-03 under 510(k) number K220466. 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 ibiomedi Electronic Stethoscope ES-2020?

ibiomedi Electronic Stethoscope ES-2020 is a medical device that received FDA 510(k) clearance on 2022-11-03. The listed applicant is Sound Land Corp.. The 510(k) number is K220466.

When did ibiomedi Electronic Stethoscope ES-2020 receive FDA 510(k) clearance?

ibiomedi Electronic Stethoscope ES-2020 received FDA 510(k) clearance on 2022-11-03, under 510(k) number K220466.

Who is the listed applicant for ibiomedi Electronic Stethoscope ES-2020?

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

What is the FDA product code for ibiomedi Electronic Stethoscope ES-2020?

The FDA product code for ibiomedi Electronic Stethoscope ES-2020 is DQD.

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