DentMix VPS印模材料
K号: K223892 · 2023-04-27
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器械摘要
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
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。
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
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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