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FDA 510(k)

DentMix VPS印模材料

K号: K223892 · 2023-04-27

决定日期2023-04-27
产品代码ELW
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决定实质等同

器械摘要

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.

常见问题

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.

相关临床试验

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列明Innovative Product Brands, Inc.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

相关器械(代码:ELW)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

官方来源

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