FDA 510(k)

Eco Abutment, Multiunit Abutment

Número K: K220253 · 2023-08-18

Data da decisão2023-08-18

Código do produtoNHA

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Eco Abutment, Multiunit Abutment is the device name listed in this FDA 510(k) record. The listed applicant is Dio Corporation. It received FDA 510(k) clearance on 2023-08-18 under 510(k) number K220253. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Eco Abutment, Multiunit Abutment?

Eco Abutment, Multiunit Abutment is a medical device that received FDA 510(k) clearance on 2023-08-18. The listed applicant is Dio Corporation. The 510(k) number is K220253.

When did Eco Abutment, Multiunit Abutment receive FDA 510(k) clearance?

Eco Abutment, Multiunit Abutment received FDA 510(k) clearance on 2023-08-18, under 510(k) number K220253.

Who is the listed applicant for Eco Abutment, Multiunit Abutment?

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

What is the FDA product code for Eco Abutment, Multiunit Abutment?

The FDA product code for Eco Abutment, Multiunit Abutment is NHA.

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Fonte oficial

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