FDA 510(k)

DentMix VPS Impression Material

Número K: K223892 · 2023-04-27

RequerenteInnovative Product Brands, Inc.

Data da decisão2023-04-27

Código do produtoELW

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

DentMix VPS Impression Material is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Product Brands, Inc.. It received FDA 510(k) clearance on 2023-04-27 under 510(k) number K223892. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the DentMix VPS Impression Material?

DentMix VPS Impression Material is a medical device that received FDA 510(k) clearance on 2023-04-27. The listed applicant is Innovative Product Brands, Inc.. The 510(k) number is K223892.

When did DentMix VPS Impression Material receive FDA 510(k) clearance?

DentMix VPS Impression Material received FDA 510(k) clearance on 2023-04-27, under 510(k) number K223892.

Who is the listed applicant for DentMix VPS Impression Material?

The FDA 510(k) record lists Innovative Product Brands, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DentMix VPS Impression Material?

The FDA product code for DentMix VPS Impression Material is ELW.

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Fonte oficial

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