FDA 510(k)

Babylog VN800, Babylog VN600

Número K: K222207 · 2023-05-16

Data da decisão2023-05-16

Código do produtoCBK

Comité consultivoAN

DecisãoSubstantially Equivalent

Resumo do dispositivo

Babylog VN800, Babylog VN600 is the device name listed in this FDA 510(k) record. The listed applicant is Draegerwerk AG & CO Kgaa. It received FDA 510(k) clearance on 2023-05-16 under 510(k) number K222207. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Babylog VN800, Babylog VN600?

Babylog VN800, Babylog VN600 is a medical device that received FDA 510(k) clearance on 2023-05-16. The listed applicant is Draegerwerk AG & CO Kgaa. The 510(k) number is K222207.

When did Babylog VN800, Babylog VN600 receive FDA 510(k) clearance?

Babylog VN800, Babylog VN600 received FDA 510(k) clearance on 2023-05-16, under 510(k) number K222207.

Who is the listed applicant for Babylog VN800, Babylog VN600?

The FDA 510(k) record lists Draegerwerk AG & CO Kgaa as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Babylog VN800, Babylog VN600?

The FDA product code for Babylog VN800, Babylog VN600 is CBK.

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Outros registros que listam Draegerwerk AG & CO Kgaa como candidato(a)

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Dispositivos Relacionados (Código: CBK)

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Fonte oficial

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